Name: rs148547109
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.

rs148547109

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:41715160 (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: C>A / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.30577 (4943/16166, ALFA)
T=0.3115 (1560/5008, 1000G)
T=0.3825 (1120/2928, KOREAN) (+ 4 more)
C=0.500 (118/236, SGDP_PRJ)
T=0.500 (118/236, SGDP_PRJ)
C=0.50 (18/36, Siberian)
T=0.50 (18/36, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MGA : 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	16166	C=0.69423	T=0.30577
European	Sub	11914	C=0.70849	T=0.29151
African	Sub	2816	C=0.6584	T=0.3416
African Others	Sub	108	C=0.620	T=0.380
African American	Sub	2708	C=0.6599	T=0.3401
Asian	Sub	108	C=0.685	T=0.315
East Asian	Sub	84	C=0.64	T=0.36
Other Asian	Sub	24	C=0.83	T=0.17
Latin American 1	Sub	146	C=0.616	T=0.384
Latin American 2	Sub	610	C=0.644	T=0.356
South Asian	Sub	94	C=0.70	T=0.30
Other	Sub	478	C=0.638	T=0.362

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	16166	C=0.69423	T=0.30577
Allele Frequency Aggregator	European	Sub	11914	C=0.70849	T=0.29151
Allele Frequency Aggregator	African	Sub	2816	C=0.6584	T=0.3416
Allele Frequency Aggregator	Latin American 2	Sub	610	C=0.644	T=0.356
Allele Frequency Aggregator	Other	Sub	478	C=0.638	T=0.362
Allele Frequency Aggregator	Latin American 1	Sub	146	C=0.616	T=0.384
Allele Frequency Aggregator	Asian	Sub	108	C=0.685	T=0.315
Allele Frequency Aggregator	South Asian	Sub	94	C=0.70	T=0.30
1000Genomes	Global	Study-wide	5008	C=0.6885	T=0.3115
1000Genomes	African	Sub	1322	C=0.6762	T=0.3238
1000Genomes	East Asian	Sub	1008	C=0.6865	T=0.3135
1000Genomes	Europe	Sub	1006	C=0.7197	T=0.2803
1000Genomes	South Asian	Sub	978	C=0.677	T=0.323
1000Genomes	American	Sub	694	C=0.686	T=0.314
KOREAN population from KRGDB	KOREAN	Study-wide	2928	C=0.6175	T=0.3825
SGDP_PRJ	Global	Study-wide	236	C=0.500	T=0.500
Siberian	Global	Study-wide	36	C=0.50	T=0.50

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 15	NC_000015.10:g.41715160C>A
GRCh38.p14 chr 15	NC_000015.10:g.41715160C>T
GRCh37.p13 chr 15	NC_000015.9:g.42007358C>A
GRCh37.p13 chr 15	NC_000015.9:g.42007358C>T

Gene: MGA, MAX dimerization protein MGA (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MGA transcript variant 2	NM_001080541.3:c.3430+166… NM_001080541.3:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant 1	NM_001164273.2:c.3430+166… NM_001164273.2:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant 3	NM_001400225.1:c.3430+166… NM_001400225.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant 4	NM_001400242.1:c.3430+166… NM_001400242.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant 5	NM_001400243.1:c.	N/A	Genic Downstream Transcript Variant
MGA transcript variant 6	NM_001400244.1:c.	N/A	Genic Downstream Transcript Variant
MGA transcript variant 7	NM_001400245.1:c.	N/A	Genic Downstream Transcript Variant
MGA transcript variant 8	NM_001400246.1:c.	N/A	Genic Downstream Transcript Variant
MGA transcript variant 9	NM_001400247.1:c.	N/A	Genic Downstream Transcript Variant
MGA transcript variant X1	XM_005254243.4:c.3430+166… XM_005254243.4:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X2	XM_005254246.4:c.3430+166… XM_005254246.4:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X6	XM_005254249.4:c.3430+166… XM_005254249.4:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X13	XM_005254252.4:c.3430+166… XM_005254252.4:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X16	XM_005254253.4:c.3430+166… XM_005254253.4:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X3	XM_006720443.5:c.3430+166… XM_006720443.5:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X30	XM_006720445.5:c.2059+166… XM_006720445.5:c.2059+1664C>A	N/A	Intron Variant
MGA transcript variant X9	XM_011521397.4:c.3430+166… XM_011521397.4:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X10	XM_011521398.4:c.3430+166… XM_011521398.4:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X29	XM_017022029.3:c.2059+166… XM_017022029.3:c.2059+1664C>A	N/A	Intron Variant
MGA transcript variant X4	XM_047432276.1:c.3430+166… XM_047432276.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X5	XM_047432278.1:c.3430+166… XM_047432278.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X7	XM_047432279.1:c.3430+166… XM_047432279.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X8	XM_047432280.1:c.3430+166… XM_047432280.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X11	XM_047432281.1:c.3430+166… XM_047432281.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X12	XM_047432282.1:c.3430+166… XM_047432282.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X14	XM_047432283.1:c.3430+166… XM_047432283.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X15	XM_047432285.1:c.3430+166… XM_047432285.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X17	XM_047432286.1:c.3430+166… XM_047432286.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X18	XM_047432287.1:c.3430+166… XM_047432287.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X19	XM_047432288.1:c.3430+166… XM_047432288.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X20	XM_047432289.1:c.3430+166… XM_047432289.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X21	XM_047432290.1:c.3430+166… XM_047432290.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X22	XM_047432291.1:c.3430+166… XM_047432291.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X23	XM_047432292.1:c.3430+166… XM_047432292.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X24	XM_047432293.1:c.3430+166… XM_047432293.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X25	XM_047432295.1:c.3430+166… XM_047432295.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X26	XM_047432296.1:c.3430+166… XM_047432296.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X27	XM_047432297.1:c.3430+166… XM_047432297.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X28	XM_047432298.1:c.3430+166… XM_047432298.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X31	XM_047432299.1:c.2059+166… XM_047432299.1:c.2059+1664C>A	N/A	Intron Variant
MGA transcript variant X32	XM_047432300.1:c.2059+166… XM_047432300.1:c.2059+1664C>A	N/A	Intron Variant
MGA transcript variant X33	XM_047432301.1:c.2059+166… XM_047432301.1:c.2059+1664C>A	N/A	Intron Variant
MGA transcript variant X34	XM_047432302.1:c.2059+166… XM_047432302.1:c.2059+1664C>A	N/A	Intron Variant
MGA transcript variant X35	XM_047432303.1:c.2059+166… XM_047432303.1:c.2059+1664C>A	N/A	Intron Variant
MGA transcript variant X36	XM_047432304.1:c.2059+166… XM_047432304.1:c.2059+1664C>A	N/A	Intron Variant
MGA transcript variant X37	XM_047432305.1:c.2059+166… XM_047432305.1:c.2059+1664C>A	N/A	Intron Variant
MGA transcript variant X38	XM_047432306.1:c.2059+166… XM_047432306.1:c.2059+1664C>A	N/A	Intron Variant
MGA transcript variant X39	XM_047432307.1:c.2059+166… XM_047432307.1:c.2059+1664C>A	N/A	Intron Variant
MGA transcript variant X40	XM_047432308.1:c.2059+166… XM_047432308.1:c.2059+1664C>A	N/A	Intron Variant
MGA transcript variant X43	XM_047432309.1:c.3430+166… XM_047432309.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X44	XM_047432310.1:c.3430+166… XM_047432310.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X45	XM_047432311.1:c.3430+166… XM_047432311.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X46	XM_047432312.1:c.3430+166… XM_047432312.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X47	XM_047432313.1:c.3430+166… XM_047432313.1:c.3430+1664C>A	N/A	Intron Variant
MGA transcript variant X41	XM_005254254.5:c.	N/A	Genic Upstream Transcript Variant
MGA transcript variant X42	XM_011521399.4: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	C=	A	T
GRCh38.p14 chr 15	NC_000015.10:g.41715160=	NC_000015.10:g.41715160C>A	NC_000015.10:g.41715160C>T
GRCh37.p13 chr 15	NC_000015.9:g.42007358=	NC_000015.9:g.42007358C>A	NC_000015.9:g.42007358C>T
MGA transcript variant 2	NM_001080541.2:c.3430+1664=	NM_001080541.2:c.3430+1664C>A	NM_001080541.2:c.3430+1664C>T
MGA transcript variant 2	NM_001080541.3:c.3430+1664=	NM_001080541.3:c.3430+1664C>A	NM_001080541.3:c.3430+1664C>T
MGA transcript variant 1	NM_001164273.1:c.3430+1664=	NM_001164273.1:c.3430+1664C>A	NM_001164273.1:c.3430+1664C>T
MGA transcript variant 1	NM_001164273.2:c.3430+1664=	NM_001164273.2:c.3430+1664C>A	NM_001164273.2:c.3430+1664C>T
MGA transcript variant 3	NM_001400225.1:c.3430+1664=	NM_001400225.1:c.3430+1664C>A	NM_001400225.1:c.3430+1664C>T
MGA transcript variant 4	NM_001400242.1:c.3430+1664=	NM_001400242.1:c.3430+1664C>A	NM_001400242.1:c.3430+1664C>T
MGA transcript variant X1	XM_005254243.1:c.3430+1664=	XM_005254243.1:c.3430+1664C>A	XM_005254243.1:c.3430+1664C>T
MGA transcript variant X1	XM_005254243.4:c.3430+1664=	XM_005254243.4:c.3430+1664C>A	XM_005254243.4:c.3430+1664C>T
MGA transcript variant X2	XM_005254244.1:c.3430+1664=	XM_005254244.1:c.3430+1664C>A	XM_005254244.1:c.3430+1664C>T
MGA transcript variant X3	XM_005254245.1:c.3430+1664=	XM_005254245.1:c.3430+1664C>A	XM_005254245.1:c.3430+1664C>T
MGA transcript variant X2	XM_005254246.1:c.3430+1664=	XM_005254246.1:c.3430+1664C>A	XM_005254246.1:c.3430+1664C>T
MGA transcript variant X2	XM_005254246.4:c.3430+1664=	XM_005254246.4:c.3430+1664C>A	XM_005254246.4:c.3430+1664C>T
MGA transcript variant X6	XM_005254247.1:c.3430+1664=	XM_005254247.1:c.3430+1664C>A	XM_005254247.1:c.3430+1664C>T
MGA transcript variant X7	XM_005254248.1:c.3430+1664=	XM_005254248.1:c.3430+1664C>A	XM_005254248.1:c.3430+1664C>T
MGA transcript variant X8	XM_005254249.1:c.3430+1664=	XM_005254249.1:c.3430+1664C>A	XM_005254249.1:c.3430+1664C>T
MGA transcript variant X6	XM_005254249.4:c.3430+1664=	XM_005254249.4:c.3430+1664C>A	XM_005254249.4:c.3430+1664C>T
MGA transcript variant X8	XM_005254250.1:c.3430+1664=	XM_005254250.1:c.3430+1664C>A	XM_005254250.1:c.3430+1664C>T
MGA transcript variant X9	XM_005254251.1:c.3430+1664=	XM_005254251.1:c.3430+1664C>A	XM_005254251.1:c.3430+1664C>T
MGA transcript variant X11	XM_005254252.1:c.3430+1664=	XM_005254252.1:c.3430+1664C>A	XM_005254252.1:c.3430+1664C>T
MGA transcript variant X13	XM_005254252.4:c.3430+1664=	XM_005254252.4:c.3430+1664C>A	XM_005254252.4:c.3430+1664C>T
MGA transcript variant X12	XM_005254253.1:c.3430+1664=	XM_005254253.1:c.3430+1664C>A	XM_005254253.1:c.3430+1664C>T
MGA transcript variant X16	XM_005254253.4:c.3430+1664=	XM_005254253.4:c.3430+1664C>A	XM_005254253.4:c.3430+1664C>T
MGA transcript variant X3	XM_006720443.5:c.3430+1664=	XM_006720443.5:c.3430+1664C>A	XM_006720443.5:c.3430+1664C>T
MGA transcript variant X30	XM_006720445.5:c.2059+1664=	XM_006720445.5:c.2059+1664C>A	XM_006720445.5:c.2059+1664C>T
MGA transcript variant X9	XM_011521397.4:c.3430+1664=	XM_011521397.4:c.3430+1664C>A	XM_011521397.4:c.3430+1664C>T
MGA transcript variant X10	XM_011521398.4:c.3430+1664=	XM_011521398.4:c.3430+1664C>A	XM_011521398.4:c.3430+1664C>T
MGA transcript variant X29	XM_017022029.3:c.2059+1664=	XM_017022029.3:c.2059+1664C>A	XM_017022029.3:c.2059+1664C>T
MGA transcript variant X4	XM_047432276.1:c.3430+1664=	XM_047432276.1:c.3430+1664C>A	XM_047432276.1:c.3430+1664C>T
MGA transcript variant X5	XM_047432278.1:c.3430+1664=	XM_047432278.1:c.3430+1664C>A	XM_047432278.1:c.3430+1664C>T
MGA transcript variant X7	XM_047432279.1:c.3430+1664=	XM_047432279.1:c.3430+1664C>A	XM_047432279.1:c.3430+1664C>T
MGA transcript variant X8	XM_047432280.1:c.3430+1664=	XM_047432280.1:c.3430+1664C>A	XM_047432280.1:c.3430+1664C>T
MGA transcript variant X11	XM_047432281.1:c.3430+1664=	XM_047432281.1:c.3430+1664C>A	XM_047432281.1:c.3430+1664C>T
MGA transcript variant X12	XM_047432282.1:c.3430+1664=	XM_047432282.1:c.3430+1664C>A	XM_047432282.1:c.3430+1664C>T
MGA transcript variant X14	XM_047432283.1:c.3430+1664=	XM_047432283.1:c.3430+1664C>A	XM_047432283.1:c.3430+1664C>T
MGA transcript variant X15	XM_047432285.1:c.3430+1664=	XM_047432285.1:c.3430+1664C>A	XM_047432285.1:c.3430+1664C>T
MGA transcript variant X17	XM_047432286.1:c.3430+1664=	XM_047432286.1:c.3430+1664C>A	XM_047432286.1:c.3430+1664C>T
MGA transcript variant X18	XM_047432287.1:c.3430+1664=	XM_047432287.1:c.3430+1664C>A	XM_047432287.1:c.3430+1664C>T
MGA transcript variant X19	XM_047432288.1:c.3430+1664=	XM_047432288.1:c.3430+1664C>A	XM_047432288.1:c.3430+1664C>T
MGA transcript variant X20	XM_047432289.1:c.3430+1664=	XM_047432289.1:c.3430+1664C>A	XM_047432289.1:c.3430+1664C>T
MGA transcript variant X21	XM_047432290.1:c.3430+1664=	XM_047432290.1:c.3430+1664C>A	XM_047432290.1:c.3430+1664C>T
MGA transcript variant X22	XM_047432291.1:c.3430+1664=	XM_047432291.1:c.3430+1664C>A	XM_047432291.1:c.3430+1664C>T
MGA transcript variant X23	XM_047432292.1:c.3430+1664=	XM_047432292.1:c.3430+1664C>A	XM_047432292.1:c.3430+1664C>T
MGA transcript variant X24	XM_047432293.1:c.3430+1664=	XM_047432293.1:c.3430+1664C>A	XM_047432293.1:c.3430+1664C>T
MGA transcript variant X25	XM_047432295.1:c.3430+1664=	XM_047432295.1:c.3430+1664C>A	XM_047432295.1:c.3430+1664C>T
MGA transcript variant X26	XM_047432296.1:c.3430+1664=	XM_047432296.1:c.3430+1664C>A	XM_047432296.1:c.3430+1664C>T
MGA transcript variant X27	XM_047432297.1:c.3430+1664=	XM_047432297.1:c.3430+1664C>A	XM_047432297.1:c.3430+1664C>T
MGA transcript variant X28	XM_047432298.1:c.3430+1664=	XM_047432298.1:c.3430+1664C>A	XM_047432298.1:c.3430+1664C>T
MGA transcript variant X31	XM_047432299.1:c.2059+1664=	XM_047432299.1:c.2059+1664C>A	XM_047432299.1:c.2059+1664C>T
MGA transcript variant X32	XM_047432300.1:c.2059+1664=	XM_047432300.1:c.2059+1664C>A	XM_047432300.1:c.2059+1664C>T
MGA transcript variant X33	XM_047432301.1:c.2059+1664=	XM_047432301.1:c.2059+1664C>A	XM_047432301.1:c.2059+1664C>T
MGA transcript variant X34	XM_047432302.1:c.2059+1664=	XM_047432302.1:c.2059+1664C>A	XM_047432302.1:c.2059+1664C>T
MGA transcript variant X35	XM_047432303.1:c.2059+1664=	XM_047432303.1:c.2059+1664C>A	XM_047432303.1:c.2059+1664C>T
MGA transcript variant X36	XM_047432304.1:c.2059+1664=	XM_047432304.1:c.2059+1664C>A	XM_047432304.1:c.2059+1664C>T
MGA transcript variant X37	XM_047432305.1:c.2059+1664=	XM_047432305.1:c.2059+1664C>A	XM_047432305.1:c.2059+1664C>T
MGA transcript variant X38	XM_047432306.1:c.2059+1664=	XM_047432306.1:c.2059+1664C>A	XM_047432306.1:c.2059+1664C>T
MGA transcript variant X39	XM_047432307.1:c.2059+1664=	XM_047432307.1:c.2059+1664C>A	XM_047432307.1:c.2059+1664C>T
MGA transcript variant X40	XM_047432308.1:c.2059+1664=	XM_047432308.1:c.2059+1664C>A	XM_047432308.1:c.2059+1664C>T
MGA transcript variant X43	XM_047432309.1:c.3430+1664=	XM_047432309.1:c.3430+1664C>A	XM_047432309.1:c.3430+1664C>T
MGA transcript variant X44	XM_047432310.1:c.3430+1664=	XM_047432310.1:c.3430+1664C>A	XM_047432310.1:c.3430+1664C>T
MGA transcript variant X45	XM_047432311.1:c.3430+1664=	XM_047432311.1:c.3430+1664C>A	XM_047432311.1:c.3430+1664C>T
MGA transcript variant X46	XM_047432312.1:c.3430+1664=	XM_047432312.1:c.3430+1664C>A	XM_047432312.1:c.3430+1664C>T
MGA transcript variant X47	XM_047432313.1:c.3430+1664=	XM_047432313.1:c.3430+1664C>A	XM_047432313.1:c.3430+1664C>T

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#.

16 SubSNP, 9 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BL	ss254932940	May 09, 2011 (134)
2	1000GENOMES	ss1353185786	Aug 21, 2014 (142)
3	USC_VALOUEV	ss2156739326	Dec 20, 2016 (150)
4	GRF	ss2701205939	Nov 08, 2017 (151)
5	SWEGEN	ss3013170334	Nov 08, 2017 (151)
6	CSHL	ss3351086142	Nov 08, 2017 (151)
7	KHV_HUMAN_GENOMES	ss3818319102	Jul 13, 2019 (153)
8	EVA	ss3834202078	Apr 27, 2020 (154)
9	SGDP_PRJ	ss3882773861	Apr 27, 2020 (154)
10	KRGDB	ss3931914757	Apr 27, 2020 (154)
11	TOMMO_GENOMICS	ss5215864139	Apr 27, 2021 (155)
12	TOMMO_GENOMICS	ss5215864140	Apr 27, 2021 (155)
13	EVA	ss5418790957	Oct 17, 2022 (156)
14	SANFORD_IMAGENETICS	ss5657373927	Oct 17, 2022 (156)
15	TOMMO_GENOMICS	ss5769571514	Oct 17, 2022 (156)
16	TOMMO_GENOMICS	ss5769571515	Oct 17, 2022 (156)
17	1000Genomes	NC_000015.9 - 42007358	Oct 12, 2018 (152)
18	KOREAN population from KRGDB	NC_000015.9 - 42007358	Apr 27, 2020 (154)
19	SGDP_PRJ	NC_000015.9 - 42007358	Apr 27, 2020 (154)
20	Siberian	NC_000015.9 - 42007358	Apr 27, 2020 (154)
21	8.3KJPN Submission ignored due to conflicting rows: Row 73833446 (NC_000015.9:42007357:C:T 1168/16752) Row 73833447 (NC_000015.9:42007357:C:A 21/16752)	-	Apr 27, 2021 (155)
22	8.3KJPN Submission ignored due to conflicting rows: Row 73833446 (NC_000015.9:42007357:C:T 1168/16752) Row 73833447 (NC_000015.9:42007357:C:A 21/16752)	-	Apr 27, 2021 (155)
23	14KJPN Submission ignored due to conflicting rows: Row 103408618 (NC_000015.10:41715159:C:T 1172/28060) Row 103408619 (NC_000015.10:41715159:C:A 69/28060)	-	Oct 17, 2022 (156)
24	14KJPN Submission ignored due to conflicting rows: Row 103408618 (NC_000015.10:41715159:C:T 1172/28060) Row 103408619 (NC_000015.10:41715159:C:A 69/28060)	-	Oct 17, 2022 (156)
25	ALFA	NC_000015.10 - 41715160	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5215864140	NC_000015.9:42007357:C:A	NC_000015.10:41715159:C:A	(self)
ss5769571515	NC_000015.10:41715159:C:A	NC_000015.10:41715159:C:A
ss254932940	NC_000015.8:39794649:C:T	NC_000015.10:41715159:C:T	(self)
66247572, 39092151, 34790841, 9255680, ss1353185786, ss2156739326, ss2701205939, ss3013170334, ss3351086142, ss3834202078, ss3882773861, ss3931914757, ss5215864139, ss5418790957, ss5657373927	NC_000015.9:42007357:C:T	NC_000015.10:41715159:C:T	(self)
5842459397, ss3818319102, ss5769571514	NC_000015.10:41715159:C:T	NC_000015.10:41715159:C:T	(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 rs148547109

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

rs148547109