Name: rs57636164
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.

rs57636164

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:70522249-70522267 (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)₈ / del(A)₇ / del(A)₆ / del(…
del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₉
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₈=0.000 (0/104, ALFA)
del(A)₇=0.000 (0/104, ALFA)
del(A)₆=0.000 (0/104, ALFA) (+ 8 more)
del(A)₅=0.000 (0/104, ALFA)
del(A)₄=0.000 (0/104, ALFA)
delAAA=0.000 (0/104, ALFA)
delAA=0.000 (0/104, ALFA)
delA=0.000 (0/104, ALFA)
dupA=0.000 (0/104, ALFA)
dupAA=0.000 (0/104, ALFA)
dupAAA=0.000 (0/104, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ADAM20 : 500B Downstream 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	104	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	40	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African	Sub	60	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	2	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	58	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	2	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	2	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A

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	104	(A)₁₉=1.000	del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	African	Sub	60	(A)₁₉=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	European	Sub	40	(A)₁₉=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	2	(A)₁₉=1.0	del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0
Allele Frequency Aggregator	Asian	Sub	2	(A)₁₉=1.0	del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0
Allele Frequency Aggregator	Latin American 2	Sub	0	(A)₁₉=0	del(A)₈=0, del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₁₉=0	del(A)₈=0, del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0
Allele Frequency Aggregator	Other	Sub	0	(A)₁₉=0	del(A)₈=0, del(A)₇=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0

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.70522260_70522267del
GRCh38.p14 chr 14	NC_000014.9:g.70522261_70522267del
GRCh38.p14 chr 14	NC_000014.9:g.70522262_70522267del
GRCh38.p14 chr 14	NC_000014.9:g.70522263_70522267del
GRCh38.p14 chr 14	NC_000014.9:g.70522264_70522267del
GRCh38.p14 chr 14	NC_000014.9:g.70522265_70522267del
GRCh38.p14 chr 14	NC_000014.9:g.70522266_70522267del
GRCh38.p14 chr 14	NC_000014.9:g.70522267del
GRCh38.p14 chr 14	NC_000014.9:g.70522267dup
GRCh38.p14 chr 14	NC_000014.9:g.70522266_70522267dup
GRCh38.p14 chr 14	NC_000014.9:g.70522265_70522267dup
GRCh38.p14 chr 14	NC_000014.9:g.70522264_70522267dup
GRCh38.p14 chr 14	NC_000014.9:g.70522263_70522267dup
GRCh38.p14 chr 14	NC_000014.9:g.70522259_70522267dup
GRCh37.p13 chr 14	NC_000014.8:g.70988977_70988984del
GRCh37.p13 chr 14	NC_000014.8:g.70988978_70988984del
GRCh37.p13 chr 14	NC_000014.8:g.70988979_70988984del
GRCh37.p13 chr 14	NC_000014.8:g.70988980_70988984del
GRCh37.p13 chr 14	NC_000014.8:g.70988981_70988984del
GRCh37.p13 chr 14	NC_000014.8:g.70988982_70988984del
GRCh37.p13 chr 14	NC_000014.8:g.70988983_70988984del
GRCh37.p13 chr 14	NC_000014.8:g.70988984del
GRCh37.p13 chr 14	NC_000014.8:g.70988984dup
GRCh37.p13 chr 14	NC_000014.8:g.70988983_70988984dup
GRCh37.p13 chr 14	NC_000014.8:g.70988982_70988984dup
GRCh37.p13 chr 14	NC_000014.8:g.70988981_70988984dup
GRCh37.p13 chr 14	NC_000014.8:g.70988980_70988984dup
GRCh37.p13 chr 14	NC_000014.8:g.70988976_70988984dup

Gene: ADAM20, ADAM metallopeptidase domain 20 (minus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
ADAM20 transcript	NM_003814.5:c.	N/A	Downstream Transcript Variant
ADAM20 transcript variant X1	XM_005268151.4:c.	N/A	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)₁₉=	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₉
GRCh38.p14 chr 14	NC_000014.9:g.70522249_70522267=	NC_000014.9:g.70522260_70522267del	NC_000014.9:g.70522261_70522267del	NC_000014.9:g.70522262_70522267del	NC_000014.9:g.70522263_70522267del	NC_000014.9:g.70522264_70522267del	NC_000014.9:g.70522265_70522267del	NC_000014.9:g.70522266_70522267del	NC_000014.9:g.70522267del	NC_000014.9:g.70522267dup	NC_000014.9:g.70522266_70522267dup	NC_000014.9:g.70522265_70522267dup	NC_000014.9:g.70522264_70522267dup	NC_000014.9:g.70522263_70522267dup	NC_000014.9:g.70522259_70522267dup
GRCh37.p13 chr 14	NC_000014.8:g.70988966_70988984=	NC_000014.8:g.70988977_70988984del	NC_000014.8:g.70988978_70988984del	NC_000014.8:g.70988979_70988984del	NC_000014.8:g.70988980_70988984del	NC_000014.8:g.70988981_70988984del	NC_000014.8:g.70988982_70988984del	NC_000014.8:g.70988983_70988984del	NC_000014.8:g.70988984del	NC_000014.8:g.70988984dup	NC_000014.8:g.70988983_70988984dup	NC_000014.8:g.70988982_70988984dup	NC_000014.8:g.70988981_70988984dup	NC_000014.8:g.70988980_70988984dup	NC_000014.8:g.70988976_70988984dup

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#.

70 SubSNP, 35 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77962800	Oct 12, 2018 (152)
2	HGSV	ss77962829	Oct 12, 2018 (152)
3	HGSV	ss77963838	Oct 12, 2018 (152)
4	HGSV	ss81603436	Sep 08, 2015 (146)
5	HGSV	ss81863549	Dec 14, 2007 (129)
6	HGSV	ss82520681	Sep 08, 2015 (146)
7	HGSV	ss82539240	Sep 08, 2015 (146)
8	HGSV	ss82782443	Sep 08, 2015 (146)
9	HUMANGENOME_JCVI	ss95644716	Dec 05, 2013 (144)
10	GMI	ss289228748	May 04, 2012 (137)
11	PJP	ss294837595	May 09, 2011 (137)
12	PJP	ss294837596	May 09, 2011 (134)
13	EVA_UK10K_ALSPAC	ss1708108639	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1708108837	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1710642234	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1710642245	Apr 01, 2015 (144)
17	SWEGEN	ss3012413777	Nov 08, 2017 (151)
18	EVA_DECODE	ss3696936551	Jul 13, 2019 (153)
19	EVA_DECODE	ss3696936552	Jul 13, 2019 (153)
20	EVA_DECODE	ss3696936553	Jul 13, 2019 (153)
21	EVA_DECODE	ss3696936554	Jul 13, 2019 (153)
22	EVA_DECODE	ss3696936555	Jul 13, 2019 (153)
23	EVA_DECODE	ss3696936556	Jul 13, 2019 (153)
24	ACPOP	ss3740497073	Jul 13, 2019 (153)
25	ACPOP	ss3740497074	Jul 13, 2019 (153)
26	ACPOP	ss3740497075	Jul 13, 2019 (153)
27	ACPOP	ss3740497076	Jul 13, 2019 (153)
28	PACBIO	ss3787701611	Jul 13, 2019 (153)
29	PACBIO	ss3792734106	Jul 13, 2019 (153)
30	PACBIO	ss3797618423	Jul 13, 2019 (153)
31	EVA	ss3833986231	Apr 27, 2020 (154)
32	GNOMAD	ss4280307900	Apr 26, 2021 (155)
33	GNOMAD	ss4280307901	Apr 26, 2021 (155)
34	GNOMAD	ss4280307902	Apr 26, 2021 (155)
35	GNOMAD	ss4280307903	Apr 26, 2021 (155)
36	GNOMAD	ss4280307904	Apr 26, 2021 (155)
37	GNOMAD	ss4280307905	Apr 26, 2021 (155)
38	GNOMAD	ss4280307906	Apr 26, 2021 (155)
39	GNOMAD	ss4280307907	Apr 26, 2021 (155)
40	GNOMAD	ss4280307908	Apr 26, 2021 (155)
41	GNOMAD	ss4280307909	Apr 26, 2021 (155)
42	GNOMAD	ss4280307910	Apr 26, 2021 (155)
43	GNOMAD	ss4280307911	Apr 26, 2021 (155)
44	GNOMAD	ss4280307912	Apr 26, 2021 (155)
45	GNOMAD	ss4280307913	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5213821174	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5213821175	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5213821176	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5213821177	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5213821178	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5213821179	Apr 26, 2021 (155)
52	1000G_HIGH_COVERAGE	ss5296680594	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5296680595	Oct 16, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5296680596	Oct 16, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5296680597	Oct 16, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5296680598	Oct 16, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5296680599	Oct 16, 2022 (156)
58	HUGCELL_USP	ss5490679348	Oct 16, 2022 (156)
59	HUGCELL_USP	ss5490679349	Oct 16, 2022 (156)
60	HUGCELL_USP	ss5490679350	Oct 16, 2022 (156)
61	HUGCELL_USP	ss5490679351	Oct 16, 2022 (156)
62	HUGCELL_USP	ss5490679352	Oct 16, 2022 (156)
63	TOMMO_GENOMICS	ss5766794066	Oct 16, 2022 (156)
64	TOMMO_GENOMICS	ss5766794067	Oct 16, 2022 (156)
65	TOMMO_GENOMICS	ss5766794068	Oct 16, 2022 (156)
66	TOMMO_GENOMICS	ss5766794069	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5766794070	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5766794071	Oct 16, 2022 (156)
69	EVA	ss5841289746	Oct 16, 2022 (156)
70	EVA	ss5841289747	Oct 16, 2022 (156)
71	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 35853877 (NC_000014.8:70988966:A: 2178/3854) Row 35853878 (NC_000014.8:70988965:AAA: 1617/3854)	-	Oct 12, 2018 (152)
72	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 35853877 (NC_000014.8:70988966:A: 2178/3854) Row 35853878 (NC_000014.8:70988965:AAA: 1617/3854)	-	Oct 12, 2018 (152)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454964239 (NC_000014.9:70522248::A 11190/101178) Row 454964240 (NC_000014.9:70522248::AA 215/101472) Row 454964241 (NC_000014.9:70522248::AAA 33/101464)...	-	Apr 26, 2021 (155)
87	Northern Sweden Submission ignored due to conflicting rows: Row 13781938 (NC_000014.8:70988965:A: 200/482) Row 13781939 (NC_000014.8:70988965:AAAAA: 20/482) Row 13781940 (NC_000014.8:70988965::A 38/482)...	-	Jul 13, 2019 (153)
88	Northern Sweden Submission ignored due to conflicting rows: Row 13781938 (NC_000014.8:70988965:A: 200/482) Row 13781939 (NC_000014.8:70988965:AAAAA: 20/482) Row 13781940 (NC_000014.8:70988965::A 38/482)...	-	Jul 13, 2019 (153)
89	Northern Sweden Submission ignored due to conflicting rows: Row 13781938 (NC_000014.8:70988965:A: 200/482) Row 13781939 (NC_000014.8:70988965:AAAAA: 20/482) Row 13781940 (NC_000014.8:70988965::A 38/482)...	-	Jul 13, 2019 (153)
90	Northern Sweden Submission ignored due to conflicting rows: Row 13781938 (NC_000014.8:70988965:A: 200/482) Row 13781939 (NC_000014.8:70988965:AAAAA: 20/482) Row 13781940 (NC_000014.8:70988965::A 38/482)...	-	Jul 13, 2019 (153)
91	8.3KJPN Submission ignored due to conflicting rows: Row 71790481 (NC_000014.8:70988965:AAAAA: 4904/16642) Row 71790482 (NC_000014.8:70988965:A: 5796/16642) Row 71790483 (NC_000014.8:70988965:AAAA: 444/16642)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 71790481 (NC_000014.8:70988965:AAAAA: 4904/16642) Row 71790482 (NC_000014.8:70988965:A: 5796/16642) Row 71790483 (NC_000014.8:70988965:AAAA: 444/16642)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 71790481 (NC_000014.8:70988965:AAAAA: 4904/16642) Row 71790482 (NC_000014.8:70988965:A: 5796/16642) Row 71790483 (NC_000014.8:70988965:AAAA: 444/16642)...	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 71790481 (NC_000014.8:70988965:AAAAA: 4904/16642) Row 71790482 (NC_000014.8:70988965:A: 5796/16642) Row 71790483 (NC_000014.8:70988965:AAAA: 444/16642)...	-	Apr 26, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 71790481 (NC_000014.8:70988965:AAAAA: 4904/16642) Row 71790482 (NC_000014.8:70988965:A: 5796/16642) Row 71790483 (NC_000014.8:70988965:AAAA: 444/16642)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 71790481 (NC_000014.8:70988965:AAAAA: 4904/16642) Row 71790482 (NC_000014.8:70988965:A: 5796/16642) Row 71790483 (NC_000014.8:70988965:AAAA: 444/16642)...	-	Apr 26, 2021 (155)
97	14KJPN Submission ignored due to conflicting rows: Row 100631170 (NC_000014.9:70522248:AAAAA: 8452/28206) Row 100631171 (NC_000014.9:70522248:A: 10727/28206) Row 100631172 (NC_000014.9:70522248:AAA: 2232/28206)...	-	Oct 16, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 100631170 (NC_000014.9:70522248:AAAAA: 8452/28206) Row 100631171 (NC_000014.9:70522248:A: 10727/28206) Row 100631172 (NC_000014.9:70522248:AAA: 2232/28206)...	-	Oct 16, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 100631170 (NC_000014.9:70522248:AAAAA: 8452/28206) Row 100631171 (NC_000014.9:70522248:A: 10727/28206) Row 100631172 (NC_000014.9:70522248:AAA: 2232/28206)...	-	Oct 16, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 100631170 (NC_000014.9:70522248:AAAAA: 8452/28206) Row 100631171 (NC_000014.9:70522248:A: 10727/28206) Row 100631172 (NC_000014.9:70522248:AAA: 2232/28206)...	-	Oct 16, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 100631170 (NC_000014.9:70522248:AAAAA: 8452/28206) Row 100631171 (NC_000014.9:70522248:A: 10727/28206) Row 100631172 (NC_000014.9:70522248:AAA: 2232/28206)...	-	Oct 16, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 100631170 (NC_000014.9:70522248:AAAAA: 8452/28206) Row 100631171 (NC_000014.9:70522248:A: 10727/28206) Row 100631172 (NC_000014.9:70522248:AAA: 2232/28206)...	-	Oct 16, 2022 (156)
103	UK 10K study - Twins Submission ignored due to conflicting rows: Row 35853877 (NC_000014.8:70988966:A: 2178/3708) Row 35853878 (NC_000014.8:70988965:AAA: 1472/3708)	-	Oct 12, 2018 (152)
104	UK 10K study - Twins Submission ignored due to conflicting rows: Row 35853877 (NC_000014.8:70988966:A: 2178/3708) Row 35853878 (NC_000014.8:70988965:AAA: 1472/3708)	-	Oct 12, 2018 (152)
105	ALFA	NC_000014.9 - 70522249	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)
rs200085700	May 11, 2012 (137)
rs143263716	May 11, 2012 (137)
rs398025569	Jul 01, 2015 (144)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4280307913	NC_000014.9:70522248:AAAAAAAA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
8785881407	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4280307912	NC_000014.9:70522248:AAAAAAA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
8785881407	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4280307911	NC_000014.9:70522248:AAAAAA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
8785881407	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3012413777, ss3740497074, ss5213821174	NC_000014.8:70988965:AAAAA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3696936556, ss4280307910, ss5296680595, ss5490679351, ss5766794066	NC_000014.9:70522248:AAAAA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
8785881407	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5213821176	NC_000014.8:70988965:AAAA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4280307909, ss5296680599, ss5766794069	NC_000014.9:70522248:AAAA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
8785881407	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3696936555	NC_000014.9:70522249:AAAA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss289228748	NC_000014.7:70058718:AAA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss81603436, ss82520681, ss82539240, ss82782443	NC_000014.7:70058734:AAA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss1708108639, ss1708108837, ss5213821178, ss5841289746	NC_000014.8:70988965:AAA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4280307908, ss5296680597, ss5490679352, ss5766794068	NC_000014.9:70522248:AAA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
8785881407	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3696936554	NC_000014.9:70522250:AAA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3740497076, ss3787701611, ss5213821179, ss5841289747	NC_000014.8:70988965:AA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss1710642234, ss1710642245	NC_000014.8:70988966:AA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4280307907, ss5296680598, ss5490679349, ss5766794071	NC_000014.9:70522248:AA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
8785881407	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3696936553	NC_000014.9:70522251:AA:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss294837595	NC_000014.7:70058718:A:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss81863549, ss294837596	NC_000014.7:70058736:A:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3740497073, ss3792734106, ss3797618423, ss3833986231, ss5213821175	NC_000014.8:70988965:A:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
	NC_000014.8:70988966:A:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4280307906, ss5296680594, ss5490679348, ss5766794067	NC_000014.9:70522248:A:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
8785881407	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3696936552	NC_000014.9:70522252:A:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss95644716	NT_026437.12:51988983:A:	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3740497075, ss5213821177	NC_000014.8:70988965::A	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4280307900, ss5296680596, ss5490679350, ss5766794070	NC_000014.9:70522248::A	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
8785881407	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3696936551	NC_000014.9:70522253::A	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss77962800, ss77962829, ss77963838	NT_026437.12:51988984::A	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4280307901	NC_000014.9:70522248::AA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
8785881407	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4280307902	NC_000014.9:70522248::AAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
8785881407	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4280307903	NC_000014.9:70522248::AAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4280307904	NC_000014.9:70522248::AAAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4280307905	NC_000014.9:70522248::AAAAAAAAA	NC_000014.9:70522248:AAAAAAAAAAAAA… NC_000014.9:70522248:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs57636164

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

rs57636164