Name: rs10700484
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs10700484

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:71972345-71972354 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: delT / dupT / dupTT / dupTTT
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.3177 (2210/6956, ALFA)
(T)₁₀=0.4453 (2230/5008, 1000G)
dupT=0.4937 (2208/4472, Estonian) (+ 4 more)
(T)₁₀=0.4754 (1832/3854, ALSPAC)
(T)₁₀=0.4571 (1695/3708, TWINSUK)
dupT=0.497 (297/598, NorthernSweden)
dupT=0.45 (18/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RGS6 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	6956	TTTTTTTTTT=0.6819	TTTTTTTTT=0.0000, TTTTTTTTTTT=0.3177, TTTTTTTTTTTT=0.0004, TTTTTTTTTTTTT=0.0000
European	Sub	5964	TTTTTTTTTT=0.6296	TTTTTTTTT=0.0000, TTTTTTTTTTT=0.3699, TTTTTTTTTTTT=0.0005, TTTTTTTTTTTTT=0.0000
African	Sub	702	TTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000
African Others	Sub	18	TTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00
African American	Sub	684	TTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000
Asian	Sub	2	TTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0
East Asian	Sub	2	TTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0
Other Asian	Sub	0	TTTTTTTTTT=0	TTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0
Latin American 1	Sub	34	TTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00
Latin American 2	Sub	144	TTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000
South Asian	Sub	18	TTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00
Other	Sub	92	TTTTTTTTTT=0.96	TTTTTTTTT=0.00, TTTTTTTTTTT=0.04, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6956	(T)₁₀=0.6819	delT=0.0000, dupT=0.3177, dupTT=0.0004, dupTTT=0.0000
Allele Frequency Aggregator	European	Sub	5964	(T)₁₀=0.6296	delT=0.0000, dupT=0.3699, dupTT=0.0005, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	702	(T)₁₀=1.000	delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	144	(T)₁₀=1.000	delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	92	(T)₁₀=0.96	delT=0.00, dupT=0.04, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	34	(T)₁₀=1.00	delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	18	(T)₁₀=1.00	delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Asian	Sub	2	(T)₁₀=1.0	delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.5547
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.4902
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.6944
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.5129
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.597
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.476
Genetic variation in the Estonian population	Estonian	Study-wide	4472	- No frequency provided	dupT=0.4937
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupT=0.5246
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupT=0.5429
Northern Sweden	ACPOP	Study-wide	598	- No frequency provided	dupT=0.497
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.45

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 14	NC_000014.9:g.71972354del
GRCh38.p14 chr 14	NC_000014.9:g.71972354dup
GRCh38.p14 chr 14	NC_000014.9:g.71972353_71972354dup
GRCh38.p14 chr 14	NC_000014.9:g.71972352_71972354dup
GRCh37.p13 chr 14	NC_000014.8:g.72439071del
GRCh37.p13 chr 14	NC_000014.8:g.72439071dup
GRCh37.p13 chr 14	NC_000014.8:g.72439070_72439071dup
GRCh37.p13 chr 14	NC_000014.8:g.72439069_72439071dup
RGS6 RefSeqGene	NG_029236.1:g.45255del
RGS6 RefSeqGene	NG_029236.1:g.45255dup
RGS6 RefSeqGene	NG_029236.1:g.45254_45255dup
RGS6 RefSeqGene	NG_029236.1:g.45253_45255dup

Gene: RGS6, regulator of G protein signaling 6 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RGS6 transcript variant 1	NM_001204416.3:c.84+7479d… NM_001204416.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 3	NM_001204417.3:c.84+7479d… NM_001204417.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 4	NM_001204418.3:c.84+7479d… NM_001204418.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 5	NM_001204419.3:c.84+7479d… NM_001204419.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 6	NM_001204420.3:c.84+7479d… NM_001204420.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 7	NM_001204421.3:c.84+7479d… NM_001204421.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 8	NM_001204422.3:c.84+7479d… NM_001204422.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 9	NM_001204423.2:c.-22+4012… NM_001204423.2:c.-22+40121del	N/A	Intron Variant
RGS6 transcript variant 10	NM_001204424.2:c.84+7479d… NM_001204424.2:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 12	NM_001370270.1:c.84+7479d… NM_001370270.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 13	NM_001370271.1:c.84+7479d… NM_001370271.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 14	NM_001370272.1:c.84+7479d… NM_001370272.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 15	NM_001370273.1:c.84+7479d… NM_001370273.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 16	NM_001370274.1:c.84+7479d… NM_001370274.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 17	NM_001370275.1:c.84+7479d… NM_001370275.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 18	NM_001370276.1:c.84+7479d… NM_001370276.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 19	NM_001370277.1:c.84+7479d… NM_001370277.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 20	NM_001370278.1:c.84+7479d… NM_001370278.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 21	NM_001370279.1:c.84+7479d… NM_001370279.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 22	NM_001370280.1:c.84+7479d… NM_001370280.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 23	NM_001370281.1:c.84+7479d… NM_001370281.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 24	NM_001370282.1:c.84+7479d… NM_001370282.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 25	NM_001370283.1:c.84+7479d… NM_001370283.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 26	NM_001370284.1:c.84+7479d… NM_001370284.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 27	NM_001370286.1:c.84+7479d… NM_001370286.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 28	NM_001370287.1:c.84+7479d… NM_001370287.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 29	NM_001370288.1:c.84+7479d… NM_001370288.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 30	NM_001370289.1:c.84+7479d… NM_001370289.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 31	NM_001370290.1:c.84+7479d… NM_001370290.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 32	NM_001370291.1:c.84+7479d… NM_001370291.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 33	NM_001370292.1:c.84+7479d… NM_001370292.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 34	NM_001370293.1:c.84+7479d… NM_001370293.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 35	NM_001370294.1:c.84+7479d… NM_001370294.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 2	NM_004296.7:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant 11	NR_135235.2:n.	N/A	Intron Variant
RGS6 transcript variant X4	XM_017021820.3:c.84+7479d… XM_017021820.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X9	XM_017021822.3:c.84+7479d… XM_017021822.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X11	XM_017021825.3:c.84+7479d… XM_017021825.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X12	XM_017021826.3:c.84+7479d… XM_017021826.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X13	XM_017021827.3:c.84+7479d… XM_017021827.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X15	XM_017021828.3:c.84+7479d… XM_017021828.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X16	XM_017021830.3:c.84+7479d… XM_017021830.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X17	XM_017021831.3:c.84+7479d… XM_017021831.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X18	XM_017021832.3:c.84+7479d… XM_017021832.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X21	XM_017021833.3:c.84+7479d… XM_017021833.3:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X1	XM_024449759.2:c.84+7479d… XM_024449759.2:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X3	XM_024449760.2:c.84+7479d… XM_024449760.2:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X2	XM_024449761.2:c.84+7479d… XM_024449761.2:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X19	XM_024449776.2:c.84+7479d… XM_024449776.2:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X10	XM_047431987.1:c.84+7479d… XM_047431987.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X20	XM_047431990.1:c.84+7479d… XM_047431990.1:c.84+7479del	N/A	Intron Variant
RGS6 transcript variant X8	XM_011537397.2:c.	N/A	Genic Upstream Transcript Variant
RGS6 transcript variant X6	XM_024449763.2:c.	N/A	Genic Upstream Transcript Variant
RGS6 transcript variant X7	XM_024449764.2:c.	N/A	Genic Upstream Transcript Variant
RGS6 transcript variant X5	XM_047431985.1:c.	N/A	Genic Upstream Transcript Variant
RGS6 transcript variant X14	XM_047431988.1:c.	N/A	Genic Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₁₀=	delT	dupT	dupTT	dupTTT
GRCh38.p14 chr 14	NC_000014.9:g.71972345_71972354=	NC_000014.9:g.71972354del	NC_000014.9:g.71972354dup	NC_000014.9:g.71972353_71972354dup	NC_000014.9:g.71972352_71972354dup
GRCh37.p13 chr 14	NC_000014.8:g.72439062_72439071=	NC_000014.8:g.72439071del	NC_000014.8:g.72439071dup	NC_000014.8:g.72439070_72439071dup	NC_000014.8:g.72439069_72439071dup
RGS6 RefSeqGene	NG_029236.1:g.45246_45255=	NG_029236.1:g.45255del	NG_029236.1:g.45255dup	NG_029236.1:g.45254_45255dup	NG_029236.1:g.45253_45255dup
RGS6 transcript variant 1	NM_001204416.1:c.84+7470=	NM_001204416.1:c.84+7479del	NM_001204416.1:c.84+7479dup	NM_001204416.1:c.84+7478_84+7479dup	NM_001204416.1:c.84+7477_84+7479dup
RGS6 transcript variant 1	NM_001204416.3:c.84+7470=	NM_001204416.3:c.84+7479del	NM_001204416.3:c.84+7479dup	NM_001204416.3:c.84+7478_84+7479dup	NM_001204416.3:c.84+7477_84+7479dup
RGS6 transcript variant 3	NM_001204417.1:c.84+7470=	NM_001204417.1:c.84+7479del	NM_001204417.1:c.84+7479dup	NM_001204417.1:c.84+7478_84+7479dup	NM_001204417.1:c.84+7477_84+7479dup
RGS6 transcript variant 3	NM_001204417.3:c.84+7470=	NM_001204417.3:c.84+7479del	NM_001204417.3:c.84+7479dup	NM_001204417.3:c.84+7478_84+7479dup	NM_001204417.3:c.84+7477_84+7479dup
RGS6 transcript variant 4	NM_001204418.1:c.84+7470=	NM_001204418.1:c.84+7479del	NM_001204418.1:c.84+7479dup	NM_001204418.1:c.84+7478_84+7479dup	NM_001204418.1:c.84+7477_84+7479dup
RGS6 transcript variant 4	NM_001204418.3:c.84+7470=	NM_001204418.3:c.84+7479del	NM_001204418.3:c.84+7479dup	NM_001204418.3:c.84+7478_84+7479dup	NM_001204418.3:c.84+7477_84+7479dup
RGS6 transcript variant 5	NM_001204419.1:c.84+7470=	NM_001204419.1:c.84+7479del	NM_001204419.1:c.84+7479dup	NM_001204419.1:c.84+7478_84+7479dup	NM_001204419.1:c.84+7477_84+7479dup
RGS6 transcript variant 5	NM_001204419.3:c.84+7470=	NM_001204419.3:c.84+7479del	NM_001204419.3:c.84+7479dup	NM_001204419.3:c.84+7478_84+7479dup	NM_001204419.3:c.84+7477_84+7479dup
RGS6 transcript variant 6	NM_001204420.1:c.84+7470=	NM_001204420.1:c.84+7479del	NM_001204420.1:c.84+7479dup	NM_001204420.1:c.84+7478_84+7479dup	NM_001204420.1:c.84+7477_84+7479dup
RGS6 transcript variant 6	NM_001204420.3:c.84+7470=	NM_001204420.3:c.84+7479del	NM_001204420.3:c.84+7479dup	NM_001204420.3:c.84+7478_84+7479dup	NM_001204420.3:c.84+7477_84+7479dup
RGS6 transcript variant 7	NM_001204421.1:c.84+7470=	NM_001204421.1:c.84+7479del	NM_001204421.1:c.84+7479dup	NM_001204421.1:c.84+7478_84+7479dup	NM_001204421.1:c.84+7477_84+7479dup
RGS6 transcript variant 7	NM_001204421.3:c.84+7470=	NM_001204421.3:c.84+7479del	NM_001204421.3:c.84+7479dup	NM_001204421.3:c.84+7478_84+7479dup	NM_001204421.3:c.84+7477_84+7479dup
RGS6 transcript variant 8	NM_001204422.1:c.84+7470=	NM_001204422.1:c.84+7479del	NM_001204422.1:c.84+7479dup	NM_001204422.1:c.84+7478_84+7479dup	NM_001204422.1:c.84+7477_84+7479dup
RGS6 transcript variant 8	NM_001204422.3:c.84+7470=	NM_001204422.3:c.84+7479del	NM_001204422.3:c.84+7479dup	NM_001204422.3:c.84+7478_84+7479dup	NM_001204422.3:c.84+7477_84+7479dup
RGS6 transcript variant 9	NM_001204423.1:c.-22+40112=	NM_001204423.1:c.-22+40121del	NM_001204423.1:c.-22+40121dup	NM_001204423.1:c.-22+40120_-22+40121dup	NM_001204423.1:c.-22+40119_-22+40121dup
RGS6 transcript variant 9	NM_001204423.2:c.-22+40112=	NM_001204423.2:c.-22+40121del	NM_001204423.2:c.-22+40121dup	NM_001204423.2:c.-22+40120_-22+40121dup	NM_001204423.2:c.-22+40119_-22+40121dup
RGS6 transcript variant 10	NM_001204424.1:c.84+7470=	NM_001204424.1:c.84+7479del	NM_001204424.1:c.84+7479dup	NM_001204424.1:c.84+7478_84+7479dup	NM_001204424.1:c.84+7477_84+7479dup
RGS6 transcript variant 10	NM_001204424.2:c.84+7470=	NM_001204424.2:c.84+7479del	NM_001204424.2:c.84+7479dup	NM_001204424.2:c.84+7478_84+7479dup	NM_001204424.2:c.84+7477_84+7479dup
RGS6 transcript variant 12	NM_001370270.1:c.84+7470=	NM_001370270.1:c.84+7479del	NM_001370270.1:c.84+7479dup	NM_001370270.1:c.84+7478_84+7479dup	NM_001370270.1:c.84+7477_84+7479dup
RGS6 transcript variant 13	NM_001370271.1:c.84+7470=	NM_001370271.1:c.84+7479del	NM_001370271.1:c.84+7479dup	NM_001370271.1:c.84+7478_84+7479dup	NM_001370271.1:c.84+7477_84+7479dup
RGS6 transcript variant 14	NM_001370272.1:c.84+7470=	NM_001370272.1:c.84+7479del	NM_001370272.1:c.84+7479dup	NM_001370272.1:c.84+7478_84+7479dup	NM_001370272.1:c.84+7477_84+7479dup
RGS6 transcript variant 15	NM_001370273.1:c.84+7470=	NM_001370273.1:c.84+7479del	NM_001370273.1:c.84+7479dup	NM_001370273.1:c.84+7478_84+7479dup	NM_001370273.1:c.84+7477_84+7479dup
RGS6 transcript variant 16	NM_001370274.1:c.84+7470=	NM_001370274.1:c.84+7479del	NM_001370274.1:c.84+7479dup	NM_001370274.1:c.84+7478_84+7479dup	NM_001370274.1:c.84+7477_84+7479dup
RGS6 transcript variant 17	NM_001370275.1:c.84+7470=	NM_001370275.1:c.84+7479del	NM_001370275.1:c.84+7479dup	NM_001370275.1:c.84+7478_84+7479dup	NM_001370275.1:c.84+7477_84+7479dup
RGS6 transcript variant 18	NM_001370276.1:c.84+7470=	NM_001370276.1:c.84+7479del	NM_001370276.1:c.84+7479dup	NM_001370276.1:c.84+7478_84+7479dup	NM_001370276.1:c.84+7477_84+7479dup
RGS6 transcript variant 19	NM_001370277.1:c.84+7470=	NM_001370277.1:c.84+7479del	NM_001370277.1:c.84+7479dup	NM_001370277.1:c.84+7478_84+7479dup	NM_001370277.1:c.84+7477_84+7479dup
RGS6 transcript variant 20	NM_001370278.1:c.84+7470=	NM_001370278.1:c.84+7479del	NM_001370278.1:c.84+7479dup	NM_001370278.1:c.84+7478_84+7479dup	NM_001370278.1:c.84+7477_84+7479dup
RGS6 transcript variant 21	NM_001370279.1:c.84+7470=	NM_001370279.1:c.84+7479del	NM_001370279.1:c.84+7479dup	NM_001370279.1:c.84+7478_84+7479dup	NM_001370279.1:c.84+7477_84+7479dup
RGS6 transcript variant 22	NM_001370280.1:c.84+7470=	NM_001370280.1:c.84+7479del	NM_001370280.1:c.84+7479dup	NM_001370280.1:c.84+7478_84+7479dup	NM_001370280.1:c.84+7477_84+7479dup
RGS6 transcript variant 23	NM_001370281.1:c.84+7470=	NM_001370281.1:c.84+7479del	NM_001370281.1:c.84+7479dup	NM_001370281.1:c.84+7478_84+7479dup	NM_001370281.1:c.84+7477_84+7479dup
RGS6 transcript variant 24	NM_001370282.1:c.84+7470=	NM_001370282.1:c.84+7479del	NM_001370282.1:c.84+7479dup	NM_001370282.1:c.84+7478_84+7479dup	NM_001370282.1:c.84+7477_84+7479dup
RGS6 transcript variant 25	NM_001370283.1:c.84+7470=	NM_001370283.1:c.84+7479del	NM_001370283.1:c.84+7479dup	NM_001370283.1:c.84+7478_84+7479dup	NM_001370283.1:c.84+7477_84+7479dup
RGS6 transcript variant 26	NM_001370284.1:c.84+7470=	NM_001370284.1:c.84+7479del	NM_001370284.1:c.84+7479dup	NM_001370284.1:c.84+7478_84+7479dup	NM_001370284.1:c.84+7477_84+7479dup
RGS6 transcript variant 27	NM_001370286.1:c.84+7470=	NM_001370286.1:c.84+7479del	NM_001370286.1:c.84+7479dup	NM_001370286.1:c.84+7478_84+7479dup	NM_001370286.1:c.84+7477_84+7479dup
RGS6 transcript variant 28	NM_001370287.1:c.84+7470=	NM_001370287.1:c.84+7479del	NM_001370287.1:c.84+7479dup	NM_001370287.1:c.84+7478_84+7479dup	NM_001370287.1:c.84+7477_84+7479dup
RGS6 transcript variant 29	NM_001370288.1:c.84+7470=	NM_001370288.1:c.84+7479del	NM_001370288.1:c.84+7479dup	NM_001370288.1:c.84+7478_84+7479dup	NM_001370288.1:c.84+7477_84+7479dup
RGS6 transcript variant 30	NM_001370289.1:c.84+7470=	NM_001370289.1:c.84+7479del	NM_001370289.1:c.84+7479dup	NM_001370289.1:c.84+7478_84+7479dup	NM_001370289.1:c.84+7477_84+7479dup
RGS6 transcript variant 31	NM_001370290.1:c.84+7470=	NM_001370290.1:c.84+7479del	NM_001370290.1:c.84+7479dup	NM_001370290.1:c.84+7478_84+7479dup	NM_001370290.1:c.84+7477_84+7479dup
RGS6 transcript variant 32	NM_001370291.1:c.84+7470=	NM_001370291.1:c.84+7479del	NM_001370291.1:c.84+7479dup	NM_001370291.1:c.84+7478_84+7479dup	NM_001370291.1:c.84+7477_84+7479dup
RGS6 transcript variant 33	NM_001370292.1:c.84+7470=	NM_001370292.1:c.84+7479del	NM_001370292.1:c.84+7479dup	NM_001370292.1:c.84+7478_84+7479dup	NM_001370292.1:c.84+7477_84+7479dup
RGS6 transcript variant 34	NM_001370293.1:c.84+7470=	NM_001370293.1:c.84+7479del	NM_001370293.1:c.84+7479dup	NM_001370293.1:c.84+7478_84+7479dup	NM_001370293.1:c.84+7477_84+7479dup
RGS6 transcript variant 35	NM_001370294.1:c.84+7470=	NM_001370294.1:c.84+7479del	NM_001370294.1:c.84+7479dup	NM_001370294.1:c.84+7478_84+7479dup	NM_001370294.1:c.84+7477_84+7479dup
RGS6 transcript variant 2	NM_004296.5:c.84+7470=	NM_004296.5:c.84+7479del	NM_004296.5:c.84+7479dup	NM_004296.5:c.84+7478_84+7479dup	NM_004296.5:c.84+7477_84+7479dup
RGS6 transcript variant 2	NM_004296.7:c.84+7470=	NM_004296.7:c.84+7479del	NM_004296.7:c.84+7479dup	NM_004296.7:c.84+7478_84+7479dup	NM_004296.7:c.84+7477_84+7479dup
RGS6 transcript variant X1	XM_005268231.1:c.84+7470=	XM_005268231.1:c.84+7479del	XM_005268231.1:c.84+7479dup	XM_005268231.1:c.84+7478_84+7479dup	XM_005268231.1:c.84+7477_84+7479dup
RGS6 transcript variant X3	XM_005268233.1:c.84+7470=	XM_005268233.1:c.84+7479del	XM_005268233.1:c.84+7479dup	XM_005268233.1:c.84+7478_84+7479dup	XM_005268233.1:c.84+7477_84+7479dup
RGS6 transcript variant X4	XM_005268234.1:c.84+7470=	XM_005268234.1:c.84+7479del	XM_005268234.1:c.84+7479dup	XM_005268234.1:c.84+7478_84+7479dup	XM_005268234.1:c.84+7477_84+7479dup
RGS6 transcript variant X5	XM_005268235.1:c.84+7470=	XM_005268235.1:c.84+7479del	XM_005268235.1:c.84+7479dup	XM_005268235.1:c.84+7478_84+7479dup	XM_005268235.1:c.84+7477_84+7479dup
RGS6 transcript variant X21	XM_005268236.1:c.84+7470=	XM_005268236.1:c.84+7479del	XM_005268236.1:c.84+7479dup	XM_005268236.1:c.84+7478_84+7479dup	XM_005268236.1:c.84+7477_84+7479dup
RGS6 transcript variant X4	XM_017021820.3:c.84+7470=	XM_017021820.3:c.84+7479del	XM_017021820.3:c.84+7479dup	XM_017021820.3:c.84+7478_84+7479dup	XM_017021820.3:c.84+7477_84+7479dup
RGS6 transcript variant X9	XM_017021822.3:c.84+7470=	XM_017021822.3:c.84+7479del	XM_017021822.3:c.84+7479dup	XM_017021822.3:c.84+7478_84+7479dup	XM_017021822.3:c.84+7477_84+7479dup
RGS6 transcript variant X11	XM_017021825.3:c.84+7470=	XM_017021825.3:c.84+7479del	XM_017021825.3:c.84+7479dup	XM_017021825.3:c.84+7478_84+7479dup	XM_017021825.3:c.84+7477_84+7479dup
RGS6 transcript variant X12	XM_017021826.3:c.84+7470=	XM_017021826.3:c.84+7479del	XM_017021826.3:c.84+7479dup	XM_017021826.3:c.84+7478_84+7479dup	XM_017021826.3:c.84+7477_84+7479dup
RGS6 transcript variant X13	XM_017021827.3:c.84+7470=	XM_017021827.3:c.84+7479del	XM_017021827.3:c.84+7479dup	XM_017021827.3:c.84+7478_84+7479dup	XM_017021827.3:c.84+7477_84+7479dup
RGS6 transcript variant X15	XM_017021828.3:c.84+7470=	XM_017021828.3:c.84+7479del	XM_017021828.3:c.84+7479dup	XM_017021828.3:c.84+7478_84+7479dup	XM_017021828.3:c.84+7477_84+7479dup
RGS6 transcript variant X16	XM_017021830.3:c.84+7470=	XM_017021830.3:c.84+7479del	XM_017021830.3:c.84+7479dup	XM_017021830.3:c.84+7478_84+7479dup	XM_017021830.3:c.84+7477_84+7479dup
RGS6 transcript variant X17	XM_017021831.3:c.84+7470=	XM_017021831.3:c.84+7479del	XM_017021831.3:c.84+7479dup	XM_017021831.3:c.84+7478_84+7479dup	XM_017021831.3:c.84+7477_84+7479dup
RGS6 transcript variant X18	XM_017021832.3:c.84+7470=	XM_017021832.3:c.84+7479del	XM_017021832.3:c.84+7479dup	XM_017021832.3:c.84+7478_84+7479dup	XM_017021832.3:c.84+7477_84+7479dup
RGS6 transcript variant X21	XM_017021833.3:c.84+7470=	XM_017021833.3:c.84+7479del	XM_017021833.3:c.84+7479dup	XM_017021833.3:c.84+7478_84+7479dup	XM_017021833.3:c.84+7477_84+7479dup
RGS6 transcript variant X1	XM_024449759.2:c.84+7470=	XM_024449759.2:c.84+7479del	XM_024449759.2:c.84+7479dup	XM_024449759.2:c.84+7478_84+7479dup	XM_024449759.2:c.84+7477_84+7479dup
RGS6 transcript variant X3	XM_024449760.2:c.84+7470=	XM_024449760.2:c.84+7479del	XM_024449760.2:c.84+7479dup	XM_024449760.2:c.84+7478_84+7479dup	XM_024449760.2:c.84+7477_84+7479dup
RGS6 transcript variant X2	XM_024449761.2:c.84+7470=	XM_024449761.2:c.84+7479del	XM_024449761.2:c.84+7479dup	XM_024449761.2:c.84+7478_84+7479dup	XM_024449761.2:c.84+7477_84+7479dup
RGS6 transcript variant X19	XM_024449776.2:c.84+7470=	XM_024449776.2:c.84+7479del	XM_024449776.2:c.84+7479dup	XM_024449776.2:c.84+7478_84+7479dup	XM_024449776.2:c.84+7477_84+7479dup
RGS6 transcript variant X10	XM_047431987.1:c.84+7470=	XM_047431987.1:c.84+7479del	XM_047431987.1:c.84+7479dup	XM_047431987.1:c.84+7478_84+7479dup	XM_047431987.1:c.84+7477_84+7479dup
RGS6 transcript variant X20	XM_047431990.1:c.84+7470=	XM_047431990.1:c.84+7479del	XM_047431990.1:c.84+7479dup	XM_047431990.1:c.84+7478_84+7479dup	XM_047431990.1:c.84+7477_84+7479dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

59 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40523746	Mar 15, 2006 (138)
2	HGSV	ss78012246	Dec 03, 2013 (138)
3	HUMANGENOME_JCVI	ss96893022	Feb 06, 2009 (137)
4	BGI	ss104701455	Feb 13, 2009 (137)
5	BGI	ss105472844	Feb 13, 2009 (137)
6	GMI	ss287920308	Dec 06, 2013 (138)
7	GMI	ss289229266	May 04, 2012 (137)
8	PJP	ss294837945	May 09, 2011 (137)
9	1000GENOMES	ss327618521	May 09, 2011 (138)
10	1000GENOMES	ss327731926	May 09, 2011 (138)
11	1000GENOMES	ss328140179	May 09, 2011 (138)
12	LUNTER	ss552373011	Apr 25, 2013 (138)
13	LUNTER	ss552704512	Apr 25, 2013 (138)
14	LUNTER	ss553554416	Apr 25, 2013 (138)
15	SSMP	ss664241239	Apr 01, 2015 (144)
16	BILGI_BIOE	ss666631533	Apr 25, 2013 (138)
17	1000GENOMES	ss1374260050	Aug 21, 2014 (142)
18	DDI	ss1536789563	Apr 01, 2015 (144)
19	EVA_GENOME_DK	ss1574781570	Apr 01, 2015 (144)
20	EVA_UK10K_ALSPAC	ss1708112793	Apr 01, 2015 (144)
21	EVA_UK10K_TWINSUK	ss1708112897	Apr 01, 2015 (144)
22	HAMMER_LAB	ss1807980890	Sep 08, 2015 (146)
23	JJLAB	ss2031237551	Sep 14, 2016 (149)
24	SWEGEN	ss3012430678	Nov 08, 2017 (151)
25	SWEGEN	ss3012430679	Nov 08, 2017 (151)
26	MCHAISSO	ss3063799369	Nov 08, 2017 (151)
27	MCHAISSO	ss3064634162	Nov 08, 2017 (151)
28	MCHAISSO	ss3065563126	Nov 08, 2017 (151)
29	BIOINF_KMB_FNS_UNIBA	ss3645354918	Oct 12, 2018 (152)
30	URBANLAB	ss3650234554	Oct 12, 2018 (152)
31	EGCUT_WGS	ss3679687385	Jul 13, 2019 (153)
32	EVA_DECODE	ss3696956311	Jul 13, 2019 (153)
33	EVA_DECODE	ss3696956312	Jul 13, 2019 (153)
34	ACPOP	ss3740506540	Jul 13, 2019 (153)
35	PACBIO	ss3787704149	Jul 13, 2019 (153)
36	PACBIO	ss3792736125	Jul 13, 2019 (153)
37	PACBIO	ss3797620455	Jul 13, 2019 (153)
38	KHV_HUMAN_GENOMES	ss3817823107	Jul 13, 2019 (153)
39	EVA	ss3833991750	Apr 27, 2020 (154)
40	EVA	ss3840587062	Apr 27, 2020 (154)
41	EVA	ss3846076573	Apr 27, 2020 (154)
42	KOGIC	ss3975208375	Apr 27, 2020 (154)
43	KOGIC	ss3975208376	Apr 27, 2020 (154)
44	GNOMAD	ss4280482872	Apr 27, 2021 (155)
45	GNOMAD	ss4280482873	Apr 27, 2021 (155)
46	GNOMAD	ss4280482874	Apr 27, 2021 (155)
47	TOMMO_GENOMICS	ss5213866499	Apr 27, 2021 (155)
48	TOMMO_GENOMICS	ss5213866500	Apr 27, 2021 (155)
49	TOMMO_GENOMICS	ss5213866501	Apr 27, 2021 (155)
50	1000G_HIGH_COVERAGE	ss5296714771	Oct 17, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5296714772	Oct 17, 2022 (156)
52	HUGCELL_USP	ss5490710396	Oct 17, 2022 (156)
53	HUGCELL_USP	ss5490710397	Oct 17, 2022 (156)
54	TOMMO_GENOMICS	ss5766852750	Oct 17, 2022 (156)
55	TOMMO_GENOMICS	ss5766852751	Oct 17, 2022 (156)
56	TOMMO_GENOMICS	ss5766852752	Oct 17, 2022 (156)
57	EVA	ss5841303753	Oct 17, 2022 (156)
58	EVA	ss5851093473	Oct 17, 2022 (156)
59	EVA	ss5947945429	Oct 17, 2022 (156)
60	1000Genomes	NC_000014.8 - 72439062	Oct 12, 2018 (152)
61	The Avon Longitudinal Study of Parents and Children	NC_000014.8 - 72439062	Oct 12, 2018 (152)
62	Genetic variation in the Estonian population	NC_000014.8 - 72439062	Oct 12, 2018 (152)
63	The Danish reference pan genome	NC_000014.8 - 72439062	Apr 27, 2020 (154)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455255265 (NC_000014.9:71972344::T 73322/137196) Row 455255266 (NC_000014.9:71972344::TT 361/137318) Row 455255267 (NC_000014.9:71972344::TTT 1/137350)	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455255265 (NC_000014.9:71972344::T 73322/137196) Row 455255266 (NC_000014.9:71972344::TT 361/137318) Row 455255267 (NC_000014.9:71972344::TTT 1/137350)	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455255265 (NC_000014.9:71972344::T 73322/137196) Row 455255266 (NC_000014.9:71972344::TT 361/137318) Row 455255267 (NC_000014.9:71972344::TTT 1/137350)	-	Apr 27, 2021 (155)
67	Korean Genome Project Submission ignored due to conflicting rows: Row 31586376 (NC_000014.9:71972344::T 1396/1832) Row 31586377 (NC_000014.9:71972344::TT 31/1832)	-	Apr 27, 2020 (154)
68	Korean Genome Project Submission ignored due to conflicting rows: Row 31586376 (NC_000014.9:71972344::T 1396/1832) Row 31586377 (NC_000014.9:71972344::TT 31/1832)	-	Apr 27, 2020 (154)
69	Northern Sweden	NC_000014.8 - 72439062	Jul 13, 2019 (153)
70	8.3KJPN Submission ignored due to conflicting rows: Row 71835806 (NC_000014.8:72439061::T 13719/16760) Row 71835807 (NC_000014.8:72439061:T: 1/16760) Row 71835808 (NC_000014.8:72439061::TT 38/16760)	-	Apr 27, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 71835806 (NC_000014.8:72439061::T 13719/16760) Row 71835807 (NC_000014.8:72439061:T: 1/16760) Row 71835808 (NC_000014.8:72439061::TT 38/16760)	-	Apr 27, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 71835806 (NC_000014.8:72439061::T 13719/16760) Row 71835807 (NC_000014.8:72439061:T: 1/16760) Row 71835808 (NC_000014.8:72439061::TT 38/16760)	-	Apr 27, 2021 (155)
73	14KJPN Submission ignored due to conflicting rows: Row 100689854 (NC_000014.9:71972344::T 23272/28258) Row 100689855 (NC_000014.9:71972344:T: 2/28258) Row 100689856 (NC_000014.9:71972344::TT 43/28258)	-	Oct 17, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 100689854 (NC_000014.9:71972344::T 23272/28258) Row 100689855 (NC_000014.9:71972344:T: 2/28258) Row 100689856 (NC_000014.9:71972344::TT 43/28258)	-	Oct 17, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 100689854 (NC_000014.9:71972344::T 23272/28258) Row 100689855 (NC_000014.9:71972344:T: 2/28258) Row 100689856 (NC_000014.9:71972344::TT 43/28258)	-	Oct 17, 2022 (156)
76	UK 10K study - Twins	NC_000014.8 - 72439062	Oct 12, 2018 (152)
77	ALFA	NC_000014.9 - 71972345	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs35407840	May 15, 2013 (138)
rs55673398	May 11, 2012 (137)
rs71855889	May 11, 2012 (137)
rs72520639	May 11, 2012 (137)
rs72573802	Feb 27, 2009 (130)
rs140100607	Sep 17, 2011 (135)
rs147081128	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5213866500	NC_000014.8:72439061:T:	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTT	(self)
ss5766852751	NC_000014.9:71972344:T:	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTT	(self)
8865821970	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTT	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTT	(self)
ss327618521, ss327731926, ss328140179, ss552373011, ss552704512, ss553554416	NC_000014.7:71508814::T	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss294837945	NC_000014.7:71508818::T	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss289229266	NC_000014.7:71508824::T	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTT	(self)
64567185, 35878107, 25425633, 459701, 13791405, 35878107, ss664241239, ss666631533, ss1374260050, ss1536789563, ss1574781570, ss1708112793, ss1708112897, ss1807980890, ss2031237551, ss3012430678, ss3679687385, ss3740506540, ss3787704149, ss3792736125, ss3797620455, ss3833991750, ss3840587062, ss5213866499, ss5841303753, ss5947945429	NC_000014.8:72439061::T	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3063799369, ss3064634162, ss3065563126, ss3645354918, ss3650234554, ss3696956311, ss3817823107, ss3846076573, ss3975208375, ss4280482872, ss5296714771, ss5490710396, ss5766852750, ss5851093473	NC_000014.9:71972344::T	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTT	(self)
8865821970	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTT	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss40523746	NT_026437.12:53439061::T	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss104701455, ss105472844	NT_026437.12:53439070::T	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss78012246, ss96893022, ss287920308	NT_026437.12:53439071::T	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3012430679, ss5213866501	NC_000014.8:72439061::TT	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3696956312, ss3975208376, ss4280482873, ss5296714772, ss5490710397, ss5766852752	NC_000014.9:71972344::TT	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTTT	(self)
8865821970	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTTT	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4280482874	NC_000014.9:71972344::TTT	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTTTT	(self)
8865821970	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTTTT	NC_000014.9:71972344:TTTTTTTTTT:TT… NC_000014.9:71972344:TTTTTTTTTT:TTTTTTTTTTTTT	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs10700484

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs10700484