Name: rs11346860
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.

rs11346860

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:163239321-163239334 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA / dup(A)₄
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.2445 (1685/6892, ALFA)
(A)₁₄=0.4687 (2347/5008, 1000G)
delA=0.482 (288/598, NorthernSweden) (+ 1 more)
(A)₁₄=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RGS5 : 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	6892	AAAAAAAAAAAAAA=0.7549	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.2445, AAAAAAAAAAAAAAA=0.0006, AAAAAAAAAAAAAAAA=0.0000
European	Sub	6348	AAAAAAAAAAAAAA=0.7341	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.2653, AAAAAAAAAAAAAAA=0.0006, AAAAAAAAAAAAAAAA=0.0000
African	Sub	92	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00
African Others	Sub	0	AAAAAAAAAAAAAA=0	AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0
African American	Sub	92	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00
Asian	Sub	64	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00
East Asian	Sub	50	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00
Other Asian	Sub	14	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00
Latin American 1	Sub	24	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00
Latin American 2	Sub	244	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000
South Asian	Sub	20	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00
Other	Sub	100	AAAAAAAAAAAAAA=0.99	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.01, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=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	6892	(A)₁₄=0.7549	delAA=0.0000, delA=0.2445, dupA=0.0006, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	6348	(A)₁₄=0.7341	delAA=0.0000, delA=0.2653, dupA=0.0006, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	244	(A)₁₄=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	100	(A)₁₄=0.99	delAA=0.00, delA=0.01, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	African	Sub	92	(A)₁₄=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	64	(A)₁₄=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	24	(A)₁₄=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	20	(A)₁₄=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₄=0.4687	delA=0.5313
1000Genomes	African	Sub	1322	(A)₁₄=0.2201	delA=0.7799
1000Genomes	East Asian	Sub	1008	(A)₁₄=0.6974	delA=0.3026
1000Genomes	Europe	Sub	1006	(A)₁₄=0.5229	delA=0.4771
1000Genomes	South Asian	Sub	978	(A)₁₄=0.454	delA=0.546
1000Genomes	American	Sub	694	(A)₁₄=0.552	delA=0.448
Northern Sweden	ACPOP	Study-wide	598	(A)₁₄=0.518	delA=0.482
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₄=0.47	delA=0.53

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 1	NC_000001.11:g.163239332_163239334del
GRCh38.p14 chr 1	NC_000001.11:g.163239333_163239334del
GRCh38.p14 chr 1	NC_000001.11:g.163239334del
GRCh38.p14 chr 1	NC_000001.11:g.163239334dup
GRCh38.p14 chr 1	NC_000001.11:g.163239333_163239334dup
GRCh38.p14 chr 1	NC_000001.11:g.163239331_163239334dup
GRCh37.p13 chr 1	NC_000001.10:g.163209122_163209124del
GRCh37.p13 chr 1	NC_000001.10:g.163209123_163209124del
GRCh37.p13 chr 1	NC_000001.10:g.163209124del
GRCh37.p13 chr 1	NC_000001.10:g.163209124dup
GRCh37.p13 chr 1	NC_000001.10:g.163209123_163209124dup
GRCh37.p13 chr 1	NC_000001.10:g.163209121_163209124dup
RGS5 RefSeqGene	NG_027731.2:g.87469_87471del
RGS5 RefSeqGene	NG_027731.2:g.87470_87471del
RGS5 RefSeqGene	NG_027731.2:g.87471del
RGS5 RefSeqGene	NG_027731.2:g.87471dup
RGS5 RefSeqGene	NG_027731.2:g.87470_87471dup
RGS5 RefSeqGene	NG_027731.2:g.87468_87471dup
TRNT1P1 pseudogene	NG_006601.2:g.2268_2270del
TRNT1P1 pseudogene	NG_006601.2:g.2269_2270del
TRNT1P1 pseudogene	NG_006601.2:g.2270del
TRNT1P1 pseudogene	NG_006601.2:g.2270dup
TRNT1P1 pseudogene	NG_006601.2:g.2269_2270dup
TRNT1P1 pseudogene	NG_006601.2:g.2267_2270dup

Gene: RGS5, regulator of G protein signaling 5 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RGS5 transcript variant 3	NM_001254748.2:c.-281+669… NM_001254748.2:c.-281+66910_-281+66912del	N/A	Intron Variant
RGS5 transcript variant 2	NM_001195303.3:c.	N/A	Genic Upstream Transcript Variant
RGS5 transcript variant 4	NM_001254749.2:c.	N/A	Genic Upstream Transcript Variant
RGS5 transcript variant 1	NM_003617.4:c.	N/A	Genic Upstream Transcript Variant
LOC127814295 transcript variant 23	NR_045630.2:n.	N/A	Genic Downstream 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	(A)₁₄=	delAAA	delAA	delA	dupA	dupAA	dup(A)₄
GRCh38.p14 chr 1	NC_000001.11:g.163239321_163239334=	NC_000001.11:g.163239332_163239334del	NC_000001.11:g.163239333_163239334del	NC_000001.11:g.163239334del	NC_000001.11:g.163239334dup	NC_000001.11:g.163239333_163239334dup	NC_000001.11:g.163239331_163239334dup
GRCh37.p13 chr 1	NC_000001.10:g.163209111_163209124=	NC_000001.10:g.163209122_163209124del	NC_000001.10:g.163209123_163209124del	NC_000001.10:g.163209124del	NC_000001.10:g.163209124dup	NC_000001.10:g.163209123_163209124dup	NC_000001.10:g.163209121_163209124dup
RGS5 RefSeqGene	NG_027731.2:g.87458_87471=	NG_027731.2:g.87469_87471del	NG_027731.2:g.87470_87471del	NG_027731.2:g.87471del	NG_027731.2:g.87471dup	NG_027731.2:g.87470_87471dup	NG_027731.2:g.87468_87471dup
TRNT1P1 pseudogene	NG_006601.2:g.2257_2270=	NG_006601.2:g.2268_2270del	NG_006601.2:g.2269_2270del	NG_006601.2:g.2270del	NG_006601.2:g.2270dup	NG_006601.2:g.2269_2270dup	NG_006601.2:g.2267_2270dup
RGS5 transcript variant 3	NM_001254748.1:c.-281+66912=	NM_001254748.1:c.-281+66910_-281+66912del	NM_001254748.1:c.-281+66911_-281+66912del	NM_001254748.1:c.-281+66912del	NM_001254748.1:c.-281+66912dup	NM_001254748.1:c.-281+66911_-281+66912dup	NM_001254748.1:c.-281+66909_-281+66912dup
RGS5 transcript variant 3	NM_001254748.2:c.-281+66912=	NM_001254748.2:c.-281+66910_-281+66912del	NM_001254748.2:c.-281+66911_-281+66912del	NM_001254748.2:c.-281+66912del	NM_001254748.2:c.-281+66912dup	NM_001254748.2:c.-281+66911_-281+66912dup	NM_001254748.2:c.-281+66909_-281+66912dup

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#.

46 SubSNP, 14 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41145560	Mar 14, 2006 (137)
2	HGSV	ss82401044	Dec 16, 2007 (129)
3	HGSV	ss83139597	Dec 16, 2007 (129)
4	BCMHGSC_JDW	ss103492279	Mar 15, 2016 (147)
5	BUSHMAN	ss193132638	Jul 04, 2010 (137)
6	PJP	ss294607693	May 09, 2011 (137)
7	PJP	ss294607694	May 09, 2011 (134)
8	SSMP	ss663127075	Apr 01, 2015 (144)
9	1000GENOMES	ss1367874998	Aug 21, 2014 (142)
10	EVA_GENOME_DK	ss1574038325	Apr 01, 2015 (144)
11	HAMMER_LAB	ss1795174645	Sep 08, 2015 (146)
12	JJLAB	ss2030353011	Sep 14, 2016 (149)
13	SWEGEN	ss2987852155	Nov 08, 2017 (151)
14	MCHAISSO	ss3064427694	Nov 08, 2017 (151)
15	MCHAISSO	ss3065331808	Nov 08, 2017 (151)
16	EVA_DECODE	ss3687901615	Jul 12, 2019 (153)
17	EVA_DECODE	ss3687901616	Jul 12, 2019 (153)
18	EVA_DECODE	ss3687901617	Jul 12, 2019 (153)
19	ACPOP	ss3727538147	Jul 12, 2019 (153)
20	PACBIO	ss3783584127	Jul 12, 2019 (153)
21	PACBIO	ss3783584128	Jul 12, 2019 (153)
22	PACBIO	ss3789212752	Jul 12, 2019 (153)
23	PACBIO	ss3794084775	Jul 12, 2019 (153)
24	KHV_HUMAN_GENOMES	ss3799881960	Jul 12, 2019 (153)
25	EVA	ss3826455777	Apr 25, 2020 (154)
26	EVA	ss3836623018	Apr 25, 2020 (154)
27	EVA	ss3842032645	Apr 25, 2020 (154)
28	KOGIC	ss3945777590	Apr 25, 2020 (154)
29	KOGIC	ss3945777591	Apr 25, 2020 (154)
30	GNOMAD	ss4004781661	Apr 25, 2021 (155)
31	GNOMAD	ss4004781662	Apr 25, 2021 (155)
32	GNOMAD	ss4004781663	Apr 25, 2021 (155)
33	GNOMAD	ss4004781664	Apr 25, 2021 (155)
34	TOMMO_GENOMICS	ss5146763273	Apr 25, 2021 (155)
35	TOMMO_GENOMICS	ss5146763274	Apr 25, 2021 (155)
36	1000G_HIGH_COVERAGE	ss5244502450	Oct 12, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5244502451	Oct 12, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5244502452	Oct 12, 2022 (156)
39	HUGCELL_USP	ss5445067027	Oct 12, 2022 (156)
40	HUGCELL_USP	ss5445067028	Oct 12, 2022 (156)
41	TOMMO_GENOMICS	ss5674043758	Oct 12, 2022 (156)
42	TOMMO_GENOMICS	ss5674043759	Oct 12, 2022 (156)
43	EVA	ss5832748665	Oct 12, 2022 (156)
44	EVA	ss5849133102	Oct 12, 2022 (156)
45	EVA	ss5910482665	Oct 12, 2022 (156)
46	EVA	ss5979994466	Oct 12, 2022 (156)
47	1000Genomes	NC_000001.10 - 163209111	Oct 11, 2018 (152)
48	The Danish reference pan genome	NC_000001.10 - 163209111	Apr 25, 2020 (154)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28802645 (NC_000001.11:163239320::A 182/130568) Row 28802646 (NC_000001.11:163239320::AA 3/130652) Row 28802647 (NC_000001.11:163239320:A: 75178/130502)...	-	Apr 25, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28802645 (NC_000001.11:163239320::A 182/130568) Row 28802646 (NC_000001.11:163239320::AA 3/130652) Row 28802647 (NC_000001.11:163239320:A: 75178/130502)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28802645 (NC_000001.11:163239320::A 182/130568) Row 28802646 (NC_000001.11:163239320::AA 3/130652) Row 28802647 (NC_000001.11:163239320:A: 75178/130502)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28802645 (NC_000001.11:163239320::A 182/130568) Row 28802646 (NC_000001.11:163239320::AA 3/130652) Row 28802647 (NC_000001.11:163239320:A: 75178/130502)...	-	Apr 25, 2021 (155)
53	Korean Genome Project Submission ignored due to conflicting rows: Row 2155591 (NC_000001.11:163239320:A: 428/1832) Row 2155592 (NC_000001.11:163239321::A 104/1832)	-	Apr 25, 2020 (154)
54	Korean Genome Project Submission ignored due to conflicting rows: Row 2155591 (NC_000001.11:163239320:A: 428/1832) Row 2155592 (NC_000001.11:163239321::A 104/1832)	-	Apr 25, 2020 (154)
55	Northern Sweden	NC_000001.10 - 163209111	Jul 12, 2019 (153)
56	8.3KJPN Submission ignored due to conflicting rows: Row 4732580 (NC_000001.10:163209110:A: 4334/16760) Row 4732581 (NC_000001.10:163209110::A 6/16760)	-	Apr 25, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 4732580 (NC_000001.10:163209110:A: 4334/16760) Row 4732581 (NC_000001.10:163209110::A 6/16760)	-	Apr 25, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 7880862 (NC_000001.11:163239320:A: 7272/28256) Row 7880863 (NC_000001.11:163239320::A 8/28256)	-	Oct 12, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 7880862 (NC_000001.11:163239320:A: 7272/28256) Row 7880863 (NC_000001.11:163239320::A 8/28256)	-	Oct 12, 2022 (156)
60	ALFA	NC_000001.11 - 163239321	Apr 25, 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)
rs79859667	Oct 15, 2011 (136)
rs34531448	May 11, 2012 (137)
rs34658814	May 11, 2012 (137)
rs374223535	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss103492279	NT_004487.19:14697763:AAA:	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3783584127	NC_000001.10:163209110:AA:	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3687901617, ss4004781664, ss5244502451	NC_000001.11:163239320:AA:	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
13974090731	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss82401044, ss83139597	NC_000001.8:159940781:A:	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss294607693	NC_000001.9:161475734:A:	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss294607694	NC_000001.9:161475747:A:	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
3966920, 176946, 823012, ss663127075, ss1367874998, ss1574038325, ss1795174645, ss2030353011, ss2987852155, ss3727538147, ss3783584128, ss3789212752, ss3794084775, ss3826455777, ss3836623018, ss5146763273, ss5832748665	NC_000001.10:163209110:A:	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3064427694, ss3065331808, ss3799881960, ss3842032645, ss3945777590, ss4004781663, ss5244502450, ss5445067027, ss5674043758, ss5849133102, ss5910482665	NC_000001.11:163239320:A:	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
13974090731	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3687901616	NC_000001.11:163239321:A:	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss41145560	NT_004487.19:14697752:A:	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss193132638	NT_004487.20:20054733:A:	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5146763274	NC_000001.10:163209110::A	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4004781661, ss5244502452, ss5445067028, ss5674043759	NC_000001.11:163239320::A	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
13974090731	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3945777591	NC_000001.11:163239321::A	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3687901615	NC_000001.11:163239322::A	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4004781662	NC_000001.11:163239320::AA	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
13974090731	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5979994466	NC_000001.10:163209110::AAAA	NC_000001.11:163239320:AAAAAAAAAAA… NC_000001.11:163239320:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA

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

No publications for rs11346860

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

rs11346860