Name: rs56239404
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.

rs56239404

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:122716899-122716916 (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: del(A)₅ / del(A)₄ / delAAA / delAA…
del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₉ / dup(A)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.2567 (1634/6366, ALFA)
(A)₁₈=0.4764 (2386/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: HCAR3 : 2KB Upstream 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	6366	AAAAAAAAAAAAAAAAAA=0.7407	AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.2567, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0008, AAAAAAAAAAAAAAAAA=0.0005, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0008, AAAAAAAAAAAAAAAAAAAAAAAA=0.0006, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.622082	0.135647	0.242271	32
European	Sub	5736	AAAAAAAAAAAAAAAAAA=0.7127	AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.2843, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0009, AAAAAAAAAAAAAAAAA=0.0005, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0009, AAAAAAAAAAAAAAAAAAAAAAAA=0.0007, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.581086	0.150263	0.268651	32
African	Sub	238	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	16	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	222	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	30	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	24	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	24	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	208	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	42	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	88	AAAAAAAAAAAAAAAAAA=0.97	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.03, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	0.954545	0.022727	0.022727	11

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6366	(A)₁₈=0.7407	delAAA=0.0000, delAA=0.2567, delA=0.0005, dupA=0.0000, dupAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0006, dup(A)₇=0.0000, dup(A)₉=0.0008, dup(A)₁₁=0.0008
Allele Frequency Aggregator	European	Sub	5736	(A)₁₈=0.7127	delAAA=0.0000, delAA=0.2843, delA=0.0005, dupA=0.0000, dupAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0007, dup(A)₇=0.0000, dup(A)₉=0.0009, dup(A)₁₁=0.0009
Allele Frequency Aggregator	African	Sub	238	(A)₁₈=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₇=0.000, dup(A)₉=0.000, dup(A)₁₁=0.000
Allele Frequency Aggregator	Latin American 2	Sub	208	(A)₁₈=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000, dup(A)₇=0.000, dup(A)₉=0.000, dup(A)₁₁=0.000
Allele Frequency Aggregator	Other	Sub	88	(A)₁₈=0.97	delAAA=0.00, delAA=0.03, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00, dup(A)₉=0.00, dup(A)₁₁=0.00
Allele Frequency Aggregator	South Asian	Sub	42	(A)₁₈=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00, dup(A)₉=0.00, dup(A)₁₁=0.00
Allele Frequency Aggregator	Asian	Sub	30	(A)₁₈=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00, dup(A)₉=0.00, dup(A)₁₁=0.00
Allele Frequency Aggregator	Latin American 1	Sub	24	(A)₁₈=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00, dup(A)₇=0.00, dup(A)₉=0.00, dup(A)₁₁=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₈=0.4764	delAA=0.5236
1000Genomes	African	Sub	1322	(A)₁₈=0.3480	delAA=0.6520
1000Genomes	East Asian	Sub	1008	(A)₁₈=0.5030	delAA=0.4970
1000Genomes	Europe	Sub	1006	(A)₁₈=0.4284	delAA=0.5716
1000Genomes	South Asian	Sub	978	(A)₁₈=0.625	delAA=0.375
1000Genomes	American	Sub	694	(A)₁₈=0.543	delAA=0.457

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 12	NC_000012.12:g.122716912_122716916del
GRCh38.p14 chr 12	NC_000012.12:g.122716913_122716916del
GRCh38.p14 chr 12	NC_000012.12:g.122716914_122716916del
GRCh38.p14 chr 12	NC_000012.12:g.122716915_122716916del
GRCh38.p14 chr 12	NC_000012.12:g.122716916del
GRCh38.p14 chr 12	NC_000012.12:g.122716916dup
GRCh38.p14 chr 12	NC_000012.12:g.122716915_122716916dup
GRCh38.p14 chr 12	NC_000012.12:g.122716914_122716916dup
GRCh38.p14 chr 12	NC_000012.12:g.122716913_122716916dup
GRCh38.p14 chr 12	NC_000012.12:g.122716912_122716916dup
GRCh38.p14 chr 12	NC_000012.12:g.122716911_122716916dup
GRCh38.p14 chr 12	NC_000012.12:g.122716910_122716916dup
GRCh38.p14 chr 12	NC_000012.12:g.122716908_122716916dup
GRCh38.p14 chr 12	NC_000012.12:g.122716906_122716916dup
GRCh37.p13 chr 12	NC_000012.11:g.123201459_123201463del
GRCh37.p13 chr 12	NC_000012.11:g.123201460_123201463del
GRCh37.p13 chr 12	NC_000012.11:g.123201461_123201463del
GRCh37.p13 chr 12	NC_000012.11:g.123201462_123201463del
GRCh37.p13 chr 12	NC_000012.11:g.123201463del
GRCh37.p13 chr 12	NC_000012.11:g.123201463dup
GRCh37.p13 chr 12	NC_000012.11:g.123201462_123201463dup
GRCh37.p13 chr 12	NC_000012.11:g.123201461_123201463dup
GRCh37.p13 chr 12	NC_000012.11:g.123201460_123201463dup
GRCh37.p13 chr 12	NC_000012.11:g.123201459_123201463dup
GRCh37.p13 chr 12	NC_000012.11:g.123201458_123201463dup
GRCh37.p13 chr 12	NC_000012.11:g.123201457_123201463dup
GRCh37.p13 chr 12	NC_000012.11:g.123201455_123201463dup
GRCh37.p13 chr 12	NC_000012.11:g.123201453_123201463dup

Gene: HCAR3, hydroxycarboxylic acid receptor 3 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
HCAR3 transcript	NM_006018.3:c.	N/A	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	(A)₁₈=	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₉	dup(A)₁₁
GRCh38.p14 chr 12	NC_000012.12:g.122716899_122716916=	NC_000012.12:g.122716912_122716916del	NC_000012.12:g.122716913_122716916del	NC_000012.12:g.122716914_122716916del	NC_000012.12:g.122716915_122716916del	NC_000012.12:g.122716916del	NC_000012.12:g.122716916dup	NC_000012.12:g.122716915_122716916dup	NC_000012.12:g.122716914_122716916dup	NC_000012.12:g.122716913_122716916dup	NC_000012.12:g.122716912_122716916dup	NC_000012.12:g.122716911_122716916dup	NC_000012.12:g.122716910_122716916dup	NC_000012.12:g.122716908_122716916dup	NC_000012.12:g.122716906_122716916dup
GRCh37.p13 chr 12	NC_000012.11:g.123201446_123201463=	NC_000012.11:g.123201459_123201463del	NC_000012.11:g.123201460_123201463del	NC_000012.11:g.123201461_123201463del	NC_000012.11:g.123201462_123201463del	NC_000012.11:g.123201463del	NC_000012.11:g.123201463dup	NC_000012.11:g.123201462_123201463dup	NC_000012.11:g.123201461_123201463dup	NC_000012.11:g.123201460_123201463dup	NC_000012.11:g.123201459_123201463dup	NC_000012.11:g.123201458_123201463dup	NC_000012.11:g.123201457_123201463dup	NC_000012.11:g.123201455_123201463dup	NC_000012.11:g.123201453_123201463dup

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#.

73 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77879113	Sep 08, 2015 (146)
2	HGSV	ss80532175	Sep 08, 2015 (146)
3	HGSV	ss80743377	Sep 08, 2015 (146)
4	HGSV	ss80746147	Sep 08, 2015 (146)
5	HGSV	ss82143473	Sep 08, 2015 (146)
6	HUMANGENOME_JCVI	ss95609959	Feb 06, 2009 (130)
7	GMI	ss289157177	May 04, 2012 (137)
8	PJP	ss294779324	Aug 21, 2014 (142)
9	PJP	ss294779325	May 09, 2011 (135)
10	SSMP	ss664097186	Apr 01, 2015 (144)
11	BILGI_BIOE	ss666586569	Apr 25, 2013 (138)
12	1000GENOMES	ss1372731151	Aug 21, 2014 (142)
13	EVA_UK10K_ALSPAC	ss1707658610	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1707658891	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1710585015	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1710585058	Apr 01, 2015 (144)
17	TMC_SNPDB	ss1997057237	Jul 19, 2016 (147)
18	SWEGEN	ss3010487154	Nov 08, 2017 (151)
19	MCHAISSO	ss3064579519	Nov 08, 2017 (151)
20	URBANLAB	ss3649938625	Oct 12, 2018 (152)
21	EVA_DECODE	ss3694638289	Jul 13, 2019 (153)
22	EVA_DECODE	ss3694638290	Jul 13, 2019 (153)
23	EVA_DECODE	ss3694638291	Jul 13, 2019 (153)
24	EVA_DECODE	ss3694638292	Jul 13, 2019 (153)
25	SANMINGWANGLAB	ss3772102408	Jul 13, 2019 (153)
26	SANMINGWANGLAB	ss3772102409	Jul 13, 2019 (153)
27	SANMINGWANGLAB	ss3772102410	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3816395863	Jul 13, 2019 (153)
29	EVA	ss3833369610	Apr 27, 2020 (154)
30	EVA	ss3840255373	Apr 27, 2020 (154)
31	EVA	ss3845744429	Apr 27, 2020 (154)
32	FSA-LAB	ss3984040088	Apr 26, 2021 (155)
33	GNOMAD	ss4260508826	Apr 26, 2021 (155)
34	GNOMAD	ss4260508827	Apr 26, 2021 (155)
35	GNOMAD	ss4260508828	Apr 26, 2021 (155)
36	GNOMAD	ss4260508829	Apr 26, 2021 (155)
37	GNOMAD	ss4260508830	Apr 26, 2021 (155)
38	GNOMAD	ss4260508831	Apr 26, 2021 (155)
39	GNOMAD	ss4260508832	Apr 26, 2021 (155)
40	GNOMAD	ss4260508833	Apr 26, 2021 (155)
41	GNOMAD	ss4260508834	Apr 26, 2021 (155)
42	GNOMAD	ss4260508835	Apr 26, 2021 (155)
43	GNOMAD	ss4260508836	Apr 26, 2021 (155)
44	GNOMAD	ss4260508837	Apr 26, 2021 (155)
45	GNOMAD	ss4260508838	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5208560946	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5208560947	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5208560948	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5208560949	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5208560950	Apr 26, 2021 (155)
51	1000G_HIGH_COVERAGE	ss5292532457	Oct 16, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5292532458	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5292532459	Oct 16, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5292532460	Oct 16, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5292532461	Oct 16, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5292532462	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5487105889	Oct 16, 2022 (156)
58	HUGCELL_USP	ss5487105890	Oct 16, 2022 (156)
59	HUGCELL_USP	ss5487105891	Oct 16, 2022 (156)
60	HUGCELL_USP	ss5487105892	Oct 16, 2022 (156)
61	EVA	ss5624037810	Oct 16, 2022 (156)
62	EVA	ss5624037811	Oct 16, 2022 (156)
63	TOMMO_GENOMICS	ss5759008636	Oct 16, 2022 (156)
64	TOMMO_GENOMICS	ss5759008637	Oct 16, 2022 (156)
65	TOMMO_GENOMICS	ss5759008638	Oct 16, 2022 (156)
66	TOMMO_GENOMICS	ss5759008639	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5759008640	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5759008641	Oct 16, 2022 (156)
69	EVA	ss5838629319	Oct 16, 2022 (156)
70	EVA	ss5838629320	Oct 16, 2022 (156)
71	TMC_SNPDB2	ss5847046208	Oct 16, 2022 (156)
72	EVA	ss5850583687	Oct 16, 2022 (156)
73	EVA	ss5980767252	Oct 16, 2022 (156)
74	1000Genomes	NC_000012.11 - 123201446	Oct 12, 2018 (152)
75	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 33211391 (NC_000012.11:123201446:A: 2647/3854) Row 33211392 (NC_000012.11:123201445:AAA: 351/3854)	-	Oct 12, 2018 (152)
76	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 33211391 (NC_000012.11:123201446:A: 2647/3854) Row 33211392 (NC_000012.11:123201445:AAA: 351/3854)	-	Oct 12, 2018 (152)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421772543 (NC_000012.12:122716898::A 2460/114024) Row 421772544 (NC_000012.12:122716898::AA 25/114058) Row 421772545 (NC_000012.12:122716898::AAA 2/114064)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421772543 (NC_000012.12:122716898::A 2460/114024) Row 421772544 (NC_000012.12:122716898::AA 25/114058) Row 421772545 (NC_000012.12:122716898::AAA 2/114064)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421772543 (NC_000012.12:122716898::A 2460/114024) Row 421772544 (NC_000012.12:122716898::AA 25/114058) Row 421772545 (NC_000012.12:122716898::AAA 2/114064)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421772543 (NC_000012.12:122716898::A 2460/114024) Row 421772544 (NC_000012.12:122716898::AA 25/114058) Row 421772545 (NC_000012.12:122716898::AAA 2/114064)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421772543 (NC_000012.12:122716898::A 2460/114024) Row 421772544 (NC_000012.12:122716898::AA 25/114058) Row 421772545 (NC_000012.12:122716898::AAA 2/114064)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421772543 (NC_000012.12:122716898::A 2460/114024) Row 421772544 (NC_000012.12:122716898::AA 25/114058) Row 421772545 (NC_000012.12:122716898::AAA 2/114064)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421772543 (NC_000012.12:122716898::A 2460/114024) Row 421772544 (NC_000012.12:122716898::AA 25/114058) Row 421772545 (NC_000012.12:122716898::AAA 2/114064)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421772543 (NC_000012.12:122716898::A 2460/114024) Row 421772544 (NC_000012.12:122716898::AA 25/114058) Row 421772545 (NC_000012.12:122716898::AAA 2/114064)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421772543 (NC_000012.12:122716898::A 2460/114024) Row 421772544 (NC_000012.12:122716898::AA 25/114058) Row 421772545 (NC_000012.12:122716898::AAA 2/114064)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421772543 (NC_000012.12:122716898::A 2460/114024) Row 421772544 (NC_000012.12:122716898::AA 25/114058) Row 421772545 (NC_000012.12:122716898::AAA 2/114064)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421772543 (NC_000012.12:122716898::A 2460/114024) Row 421772544 (NC_000012.12:122716898::AA 25/114058) Row 421772545 (NC_000012.12:122716898::AAA 2/114064)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421772543 (NC_000012.12:122716898::A 2460/114024) Row 421772544 (NC_000012.12:122716898::AA 25/114058) Row 421772545 (NC_000012.12:122716898::AAA 2/114064)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421772543 (NC_000012.12:122716898::A 2460/114024) Row 421772544 (NC_000012.12:122716898::AA 25/114058) Row 421772545 (NC_000012.12:122716898::AAA 2/114064)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 66530253 (NC_000012.11:123201445:AA: 8402/16638) Row 66530254 (NC_000012.11:123201445::AAAAAA 196/16638) Row 66530255 (NC_000012.11:123201445::A 55/16638)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 66530253 (NC_000012.11:123201445:AA: 8402/16638) Row 66530254 (NC_000012.11:123201445::AAAAAA 196/16638) Row 66530255 (NC_000012.11:123201445::A 55/16638)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 66530253 (NC_000012.11:123201445:AA: 8402/16638) Row 66530254 (NC_000012.11:123201445::AAAAAA 196/16638) Row 66530255 (NC_000012.11:123201445::A 55/16638)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 66530253 (NC_000012.11:123201445:AA: 8402/16638) Row 66530254 (NC_000012.11:123201445::AAAAAA 196/16638) Row 66530255 (NC_000012.11:123201445::A 55/16638)...	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 66530253 (NC_000012.11:123201445:AA: 8402/16638) Row 66530254 (NC_000012.11:123201445::AAAAAA 196/16638) Row 66530255 (NC_000012.11:123201445::A 55/16638)...	-	Apr 26, 2021 (155)
95	14KJPN Submission ignored due to conflicting rows: Row 92845740 (NC_000012.12:122716898:AA: 15124/28226) Row 92845741 (NC_000012.12:122716898:AAA: 32/28226) Row 92845742 (NC_000012.12:122716898::A 116/28226)...	-	Oct 16, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 92845740 (NC_000012.12:122716898:AA: 15124/28226) Row 92845741 (NC_000012.12:122716898:AAA: 32/28226) Row 92845742 (NC_000012.12:122716898::A 116/28226)...	-	Oct 16, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 92845740 (NC_000012.12:122716898:AA: 15124/28226) Row 92845741 (NC_000012.12:122716898:AAA: 32/28226) Row 92845742 (NC_000012.12:122716898::A 116/28226)...	-	Oct 16, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 92845740 (NC_000012.12:122716898:AA: 15124/28226) Row 92845741 (NC_000012.12:122716898:AAA: 32/28226) Row 92845742 (NC_000012.12:122716898::A 116/28226)...	-	Oct 16, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 92845740 (NC_000012.12:122716898:AA: 15124/28226) Row 92845741 (NC_000012.12:122716898:AAA: 32/28226) Row 92845742 (NC_000012.12:122716898::A 116/28226)...	-	Oct 16, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 92845740 (NC_000012.12:122716898:AA: 15124/28226) Row 92845741 (NC_000012.12:122716898:AAA: 32/28226) Row 92845742 (NC_000012.12:122716898::A 116/28226)...	-	Oct 16, 2022 (156)
101	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33211391 (NC_000012.11:123201446:A: 2545/3708) Row 33211392 (NC_000012.11:123201445:AAA: 305/3708)	-	Oct 12, 2018 (152)
102	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33211391 (NC_000012.11:123201446:A: 2545/3708) Row 33211392 (NC_000012.11:123201445:AAA: 305/3708)	-	Oct 12, 2018 (152)
103	ALFA	NC_000012.12 - 122716899	Apr 26, 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)
rs60335672	May 25, 2008 (130)
rs143621989	Sep 17, 2011 (135)
rs201304221	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4260508838	NC_000012.12:122716898:AAAAA:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4260508837, ss5847046208	NC_000012.12:122716898:AAAA:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss1707658610, ss1707658891, ss3984040088, ss5208560949, ss5838629320	NC_000012.11:123201445:AAA:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3694638292, ss4260508836, ss5292532461, ss5487105889, ss5759008637	NC_000012.12:122716898:AAA:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
7421509815	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss77879113, ss80532175, ss80743377, ss80746147, ss82143473	NC_000012.9:121726341:AA:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss289157177, ss294779324	NC_000012.10:121767398:AA:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss294779325	NC_000012.10:121767414:AA:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
59793423, ss664097186, ss666586569, ss1372731151, ss3010487154, ss3833369610, ss3840255373, ss5208560946, ss5624037811, ss5838629319, ss5980767252	NC_000012.11:123201445:AA:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss1710585015, ss1710585058, ss3772102409	NC_000012.11:123201446:AA:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3064579519, ss3649938625, ss3816395863, ss3845744429, ss4260508835, ss5292532457, ss5487105890, ss5759008636, ss5850583687	NC_000012.12:122716898:AA:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
7421509815	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3694638291	NC_000012.12:122716899:AA:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss95609959	NT_009755.19:620838:AA:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss1997057237, ss5208560950, ss5624037810	NC_000012.11:123201445:A:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3772102408	NC_000012.11:123201446:A:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3772102410	NC_000012.11:123201447:A:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4260508834, ss5292532458, ss5487105891, ss5759008640	NC_000012.12:122716898:A:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
7421509815	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3694638290	NC_000012.12:122716900:A:	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5208560948	NC_000012.11:123201445::A	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4260508826, ss5292532459, ss5487105892, ss5759008638	NC_000012.12:122716898::A	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
7421509815	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3694638289	NC_000012.12:122716901::A	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4260508827	NC_000012.12:122716898::AA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
7421509815	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4260508828	NC_000012.12:122716898::AAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4260508829	NC_000012.12:122716898::AAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
7421509815	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260508830, ss5292532462	NC_000012.12:122716898::AAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
7421509815	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5208560947	NC_000012.11:123201445::AAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260508831, ss5292532460, ss5759008639	NC_000012.12:122716898::AAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
7421509815	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260508832, ss5759008641	NC_000012.12:122716898::AAAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
7421509815	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
7421509815	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260508833	NC_000012.12:122716898::AAAAAAAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
7421509815	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:122716898:AAAAAAAAAAA… NC_000012.12:122716898:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs56239404

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

rs56239404