Name: rs35587006
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.

rs35587006

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:28877669-28877689 (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)₁₂ / del(A)₁₁ / del(A)₁₀ / d…
del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆
Variation Type: Indel Insertion and Deletion
Frequency: (A)₂₁=0.3612 (1809/5008, 1000G)
del(A)₁₂=0.00 (0/78, ALFA)
del(A)₉=0.00 (0/78, ALFA) (+ 9 more)
del(A)₈=0.00 (0/78, ALFA)
del(A)₇=0.00 (0/78, ALFA)
del(A)₅=0.00 (0/78, ALFA)
del(A)₄=0.00 (0/78, ALFA)
delAAA=0.00 (0/78, ALFA)
delAA=0.00 (0/78, ALFA)
delA=0.00 (0/78, ALFA)
dupA=0.00 (0/78, ALFA)
dupAA=0.00 (0/78, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: C10orf126 : 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	78	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
European	Sub	2	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African	Sub	74	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	4	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	70	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 2	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	2	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₂₁=0.3612	delAA=0.6388
1000Genomes	African	Sub	1322	(A)₂₁=0.6604	delAA=0.3396
1000Genomes	East Asian	Sub	1008	(A)₂₁=0.1429	delAA=0.8571
1000Genomes	Europe	Sub	1006	(A)₂₁=0.1829	delAA=0.8171
1000Genomes	South Asian	Sub	978	(A)₂₁=0.388	delAA=0.612
1000Genomes	American	Sub	694	(A)₂₁=0.330	delAA=0.670
Allele Frequency Aggregator	Total	Global	78	(A)₂₁=1.00	del(A)₁₂=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=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
Allele Frequency Aggregator	African	Sub	74	(A)₂₁=1.00	del(A)₁₂=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=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
Allele Frequency Aggregator	European	Sub	2	(A)₂₁=1.0	del(A)₁₂=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=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
Allele Frequency Aggregator	Other	Sub	2	(A)₂₁=1.0	del(A)₁₂=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=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
Allele Frequency Aggregator	Latin American 1	Sub	0	(A)₂₁=0	del(A)₁₂=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0
Allele Frequency Aggregator	Latin American 2	Sub	0	(A)₂₁=0	del(A)₁₂=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₂₁=0	del(A)₁₂=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0
Allele Frequency Aggregator	Asian	Sub	0	(A)₂₁=0	del(A)₁₂=0, del(A)₉=0, del(A)₈=0, del(A)₇=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=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 10	NC_000010.11:g.28877678_28877689del
GRCh38.p14 chr 10	NC_000010.11:g.28877679_28877689del
GRCh38.p14 chr 10	NC_000010.11:g.28877680_28877689del
GRCh38.p14 chr 10	NC_000010.11:g.28877681_28877689del
GRCh38.p14 chr 10	NC_000010.11:g.28877682_28877689del
GRCh38.p14 chr 10	NC_000010.11:g.28877683_28877689del
GRCh38.p14 chr 10	NC_000010.11:g.28877685_28877689del
GRCh38.p14 chr 10	NC_000010.11:g.28877686_28877689del
GRCh38.p14 chr 10	NC_000010.11:g.28877687_28877689del
GRCh38.p14 chr 10	NC_000010.11:g.28877688_28877689del
GRCh38.p14 chr 10	NC_000010.11:g.28877689del
GRCh38.p14 chr 10	NC_000010.11:g.28877689dup
GRCh38.p14 chr 10	NC_000010.11:g.28877688_28877689dup
GRCh38.p14 chr 10	NC_000010.11:g.28877687_28877689dup
GRCh38.p14 chr 10	NC_000010.11:g.28877686_28877689dup
GRCh38.p14 chr 10	NC_000010.11:g.28877685_28877689dup
GRCh38.p14 chr 10	NC_000010.11:g.28877684_28877689dup
GRCh37.p13 chr 10	NC_000010.10:g.29166607_29166618del
GRCh37.p13 chr 10	NC_000010.10:g.29166608_29166618del
GRCh37.p13 chr 10	NC_000010.10:g.29166609_29166618del
GRCh37.p13 chr 10	NC_000010.10:g.29166610_29166618del
GRCh37.p13 chr 10	NC_000010.10:g.29166611_29166618del
GRCh37.p13 chr 10	NC_000010.10:g.29166612_29166618del
GRCh37.p13 chr 10	NC_000010.10:g.29166614_29166618del
GRCh37.p13 chr 10	NC_000010.10:g.29166615_29166618del
GRCh37.p13 chr 10	NC_000010.10:g.29166616_29166618del
GRCh37.p13 chr 10	NC_000010.10:g.29166617_29166618del
GRCh37.p13 chr 10	NC_000010.10:g.29166618del
GRCh37.p13 chr 10	NC_000010.10:g.29166618dup
GRCh37.p13 chr 10	NC_000010.10:g.29166617_29166618dup
GRCh37.p13 chr 10	NC_000010.10:g.29166616_29166618dup
GRCh37.p13 chr 10	NC_000010.10:g.29166615_29166618dup
GRCh37.p13 chr 10	NC_000010.10:g.29166614_29166618dup
GRCh37.p13 chr 10	NC_000010.10:g.29166613_29166618dup

Gene: C10orf126, chromosome 10 open reading frame 126 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
C10orf126 transcript	NR_164114.1:n.	N/A	Intron 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)₂₁=	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆
GRCh38.p14 chr 10	NC_000010.11:g.28877669_28877689=	NC_000010.11:g.28877678_28877689del	NC_000010.11:g.28877679_28877689del	NC_000010.11:g.28877680_28877689del	NC_000010.11:g.28877681_28877689del	NC_000010.11:g.28877682_28877689del	NC_000010.11:g.28877683_28877689del	NC_000010.11:g.28877685_28877689del	NC_000010.11:g.28877686_28877689del	NC_000010.11:g.28877687_28877689del	NC_000010.11:g.28877688_28877689del	NC_000010.11:g.28877689del	NC_000010.11:g.28877689dup	NC_000010.11:g.28877688_28877689dup	NC_000010.11:g.28877687_28877689dup	NC_000010.11:g.28877686_28877689dup	NC_000010.11:g.28877685_28877689dup	NC_000010.11:g.28877684_28877689dup
GRCh37.p13 chr 10	NC_000010.10:g.29166598_29166618=	NC_000010.10:g.29166607_29166618del	NC_000010.10:g.29166608_29166618del	NC_000010.10:g.29166609_29166618del	NC_000010.10:g.29166610_29166618del	NC_000010.10:g.29166611_29166618del	NC_000010.10:g.29166612_29166618del	NC_000010.10:g.29166614_29166618del	NC_000010.10:g.29166615_29166618del	NC_000010.10:g.29166616_29166618del	NC_000010.10:g.29166617_29166618del	NC_000010.10:g.29166618del	NC_000010.10:g.29166618dup	NC_000010.10:g.29166617_29166618dup	NC_000010.10:g.29166616_29166618dup	NC_000010.10:g.29166615_29166618dup	NC_000010.10:g.29166614_29166618dup	NC_000010.10:g.29166613_29166618dup
C10orf126 transcript	NM_001278522.1:c.211-2469=	NM_001278522.1:c.211-2460_211-2449del	NM_001278522.1:c.211-2459_211-2449del	NM_001278522.1:c.211-2458_211-2449del	NM_001278522.1:c.211-2457_211-2449del	NM_001278522.1:c.211-2456_211-2449del	NM_001278522.1:c.211-2455_211-2449del	NM_001278522.1:c.211-2453_211-2449del	NM_001278522.1:c.211-2452_211-2449del	NM_001278522.1:c.211-2451_211-2449del	NM_001278522.1:c.211-2450_211-2449del	NM_001278522.1:c.211-2449del	NM_001278522.1:c.211-2449dup	NM_001278522.1:c.211-2450_211-2449dup	NM_001278522.1:c.211-2451_211-2449dup	NM_001278522.1:c.211-2452_211-2449dup	NM_001278522.1:c.211-2453_211-2449dup	NM_001278522.1:c.211-2454_211-2449dup

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#.

57 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss39743806	Dec 03, 2013 (138)
2	ABI	ss39823288	Mar 15, 2016 (147)
3	HUMANGENOME_JCVI	ss95537045	Feb 04, 2009 (130)
4	BCMHGSC_JDW	ss103506735	Mar 15, 2016 (147)
5	GMI	ss289005006	May 04, 2012 (144)
6	PJP	ss294649400	Aug 21, 2014 (144)
7	PJP	ss294649401	May 09, 2011 (144)
8	1000GENOMES	ss1369300277	Aug 21, 2014 (144)
9	EVA_UK10K_ALSPAC	ss1706689153	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1706689184	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710460674	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1710460676	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1710460998	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1710460999	Apr 01, 2015 (144)
15	SWEGEN	ss3006171070	Nov 08, 2017 (151)
16	MCHAISSO	ss3064466100	Nov 08, 2017 (151)
17	EVA_DECODE	ss3689565071	Jul 13, 2019 (153)
18	EVA_DECODE	ss3689565072	Jul 13, 2019 (153)
19	EVA_DECODE	ss3689565073	Jul 13, 2019 (153)
20	EVA_DECODE	ss3689565074	Jul 13, 2019 (153)
21	EVA_DECODE	ss3689565075	Jul 13, 2019 (153)
22	ACPOP	ss3737188182	Jul 13, 2019 (153)
23	ACPOP	ss3737188183	Jul 13, 2019 (153)
24	ACPOP	ss3737188184	Jul 13, 2019 (153)
25	PACBIO	ss3786625039	Jul 13, 2019 (153)
26	PACBIO	ss3791811987	Jul 13, 2019 (153)
27	PACBIO	ss3796693986	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3813285232	Jul 13, 2019 (153)
29	EVA	ss3832044616	Apr 26, 2020 (154)
30	GNOMAD	ss4215309152	Apr 26, 2021 (155)
31	GNOMAD	ss4215309153	Apr 26, 2021 (155)
32	GNOMAD	ss4215309154	Apr 26, 2021 (155)
33	GNOMAD	ss4215309155	Apr 26, 2021 (155)
34	GNOMAD	ss4215309156	Apr 26, 2021 (155)
35	GNOMAD	ss4215309157	Apr 26, 2021 (155)
36	GNOMAD	ss4215309158	Apr 26, 2021 (155)
37	GNOMAD	ss4215309159	Apr 26, 2021 (155)
38	GNOMAD	ss4215309160	Apr 26, 2021 (155)
39	GNOMAD	ss4215309161	Apr 26, 2021 (155)
40	GNOMAD	ss4215309162	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5196898033	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5196898034	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5196898035	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5196898036	Apr 26, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5283420057	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5283420058	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5283420059	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5479141229	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5479141230	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5479141231	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5741934476	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5741934477	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5741934478	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5741934479	Oct 16, 2022 (156)
55	EVA	ss5824175176	Oct 16, 2022 (156)
56	EVA	ss5824175177	Oct 16, 2022 (156)
57	EVA	ss5849501864	Oct 16, 2022 (156)
58	1000Genomes	NC_000010.10 - 29166598	Oct 12, 2018 (152)
59	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 27338088 (NC_000010.10:29166598:AA: 762/3854) Row 27338089 (NC_000010.10:29166597:AAAA: 120/3854)	-	Oct 12, 2018 (152)
60	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 27338088 (NC_000010.10:29166598:AA: 762/3854) Row 27338089 (NC_000010.10:29166597:AAAA: 120/3854)	-	Oct 12, 2018 (152)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 347406594 (NC_000010.11:28877668::A 81/82392) Row 347406595 (NC_000010.11:28877668::AA 11/82420) Row 347406596 (NC_000010.11:28877668::AAA 6/82506)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 347406594 (NC_000010.11:28877668::A 81/82392) Row 347406595 (NC_000010.11:28877668::AA 11/82420) Row 347406596 (NC_000010.11:28877668::AAA 6/82506)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 347406594 (NC_000010.11:28877668::A 81/82392) Row 347406595 (NC_000010.11:28877668::AA 11/82420) Row 347406596 (NC_000010.11:28877668::AAA 6/82506)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 347406594 (NC_000010.11:28877668::A 81/82392) Row 347406595 (NC_000010.11:28877668::AA 11/82420) Row 347406596 (NC_000010.11:28877668::AAA 6/82506)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 347406594 (NC_000010.11:28877668::A 81/82392) Row 347406595 (NC_000010.11:28877668::AA 11/82420) Row 347406596 (NC_000010.11:28877668::AAA 6/82506)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 347406594 (NC_000010.11:28877668::A 81/82392) Row 347406595 (NC_000010.11:28877668::AA 11/82420) Row 347406596 (NC_000010.11:28877668::AAA 6/82506)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 347406594 (NC_000010.11:28877668::A 81/82392) Row 347406595 (NC_000010.11:28877668::AA 11/82420) Row 347406596 (NC_000010.11:28877668::AAA 6/82506)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 347406594 (NC_000010.11:28877668::A 81/82392) Row 347406595 (NC_000010.11:28877668::AA 11/82420) Row 347406596 (NC_000010.11:28877668::AAA 6/82506)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 347406594 (NC_000010.11:28877668::A 81/82392) Row 347406595 (NC_000010.11:28877668::AA 11/82420) Row 347406596 (NC_000010.11:28877668::AAA 6/82506)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 347406594 (NC_000010.11:28877668::A 81/82392) Row 347406595 (NC_000010.11:28877668::AA 11/82420) Row 347406596 (NC_000010.11:28877668::AAA 6/82506)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 347406594 (NC_000010.11:28877668::A 81/82392) Row 347406595 (NC_000010.11:28877668::AA 11/82420) Row 347406596 (NC_000010.11:28877668::AAA 6/82506)...	-	Apr 26, 2021 (155)
72	Northern Sweden Submission ignored due to conflicting rows: Row 10473047 (NC_000010.10:29166597:AA: 290/554) Row 10473048 (NC_000010.10:29166597:A: 48/554) Row 10473049 (NC_000010.10:29166597::AAAA 7/554)	-	Jul 13, 2019 (153)
73	Northern Sweden Submission ignored due to conflicting rows: Row 10473047 (NC_000010.10:29166597:AA: 290/554) Row 10473048 (NC_000010.10:29166597:A: 48/554) Row 10473049 (NC_000010.10:29166597::AAAA 7/554)	-	Jul 13, 2019 (153)
74	Northern Sweden Submission ignored due to conflicting rows: Row 10473047 (NC_000010.10:29166597:AA: 290/554) Row 10473048 (NC_000010.10:29166597:A: 48/554) Row 10473049 (NC_000010.10:29166597::AAAA 7/554)	-	Jul 13, 2019 (153)
75	8.3KJPN Submission ignored due to conflicting rows: Row 54867340 (NC_000010.10:29166597:AA: 11792/16360) Row 54867341 (NC_000010.10:29166597:A: 2072/16360) Row 54867342 (NC_000010.10:29166597:AAA: 30/16360)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 54867340 (NC_000010.10:29166597:AA: 11792/16360) Row 54867341 (NC_000010.10:29166597:A: 2072/16360) Row 54867342 (NC_000010.10:29166597:AAA: 30/16360)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 54867340 (NC_000010.10:29166597:AA: 11792/16360) Row 54867341 (NC_000010.10:29166597:A: 2072/16360) Row 54867342 (NC_000010.10:29166597:AAA: 30/16360)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 54867340 (NC_000010.10:29166597:AA: 11792/16360) Row 54867341 (NC_000010.10:29166597:A: 2072/16360) Row 54867342 (NC_000010.10:29166597:AAA: 30/16360)...	-	Apr 26, 2021 (155)
79	14KJPN Submission ignored due to conflicting rows: Row 75771580 (NC_000010.11:28877668:A: 3962/28140) Row 75771581 (NC_000010.11:28877668:AA: 21675/28140) Row 75771582 (NC_000010.11:28877668:AAA: 53/28140)...	-	Oct 16, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 75771580 (NC_000010.11:28877668:A: 3962/28140) Row 75771581 (NC_000010.11:28877668:AA: 21675/28140) Row 75771582 (NC_000010.11:28877668:AAA: 53/28140)...	-	Oct 16, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 75771580 (NC_000010.11:28877668:A: 3962/28140) Row 75771581 (NC_000010.11:28877668:AA: 21675/28140) Row 75771582 (NC_000010.11:28877668:AAA: 53/28140)...	-	Oct 16, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 75771580 (NC_000010.11:28877668:A: 3962/28140) Row 75771581 (NC_000010.11:28877668:AA: 21675/28140) Row 75771582 (NC_000010.11:28877668:AAA: 53/28140)...	-	Oct 16, 2022 (156)
83	UK 10K study - Twins Submission ignored due to conflicting rows: Row 27338087 (NC_000010.10:29166599:AA: 2802/3708) Row 27338088 (NC_000010.10:29166598:AAA: 769/3708) Row 27338089 (NC_000010.10:29166597:AAAA: 135/3708)	-	Apr 26, 2020 (154)
84	UK 10K study - Twins Submission ignored due to conflicting rows: Row 27338088 (NC_000010.10:29166598:AA: 769/3708) Row 27338089 (NC_000010.10:29166597:AAAA: 135/3708)	-	Oct 12, 2018 (152)
85	UK 10K study - Twins Submission ignored due to conflicting rows: Row 27338088 (NC_000010.10:29166598:AA: 769/3708) Row 27338089 (NC_000010.10:29166597:AAAA: 135/3708)	-	Oct 12, 2018 (152)
86	ALFA	NC_000010.11 - 28877669	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)
rs80182976	May 11, 2012 (137)
rs72469138	May 11, 2012 (137)
rs143402248	Jul 01, 2015 (144)
rs201588241	May 11, 2012 (137)
rs35364654	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4215309162	NC_000010.11:28877668:AAAAAAAAAAAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
7690000379	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss3006171070	NC_000010.10:29166597:AAAAAAAAAAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss5196898036	NC_000010.10:29166597:AAAAAAAAAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss5741934479	NC_000010.11:28877668:AAAAAAAAAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA
ss4215309161	NC_000010.11:28877668:AAAAAAAAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
7690000379	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
7690000379	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
7690000379	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3689565075, ss4215309160	NC_000010.11:28877668:AAAAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
7690000379	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss1706689153, ss1706689184	NC_000010.10:29166597:AAAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4215309159	NC_000010.11:28877668:AAAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
7690000379	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3689565074	NC_000010.11:28877669:AAAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss103506735	NT_008705.16:29106614:AAAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3786625039, ss5196898035, ss5824175177	NC_000010.10:29166597:AAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss1710460676, ss1710460999	NC_000010.10:29166598:AAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4215309158, ss5283420059, ss5479141229, ss5741934478	NC_000010.11:28877668:AAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
7690000379	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3689565073	NC_000010.11:28877670:AAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss289005006, ss294649400	NC_000010.9:29206603:AA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss294649401	NC_000010.9:29206622:AA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
49198773, ss1369300277, ss3737188182, ss3791811987, ss3796693986, ss3832044616, ss5196898033, ss5824175176	NC_000010.10:29166597:AA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
	NC_000010.10:29166598:AA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss1710460674, ss1710460998	NC_000010.10:29166599:AA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3064466100, ss3813285232, ss4215309157, ss5283420057, ss5479141230, ss5741934477, ss5849501864	NC_000010.11:28877668:AA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
7690000379	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3689565072	NC_000010.11:28877671:AA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss39823288, ss95537045	NT_008705.16:29106616:AA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3737188183, ss5196898034	NC_000010.10:29166597:A:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5283420058, ss5479141231, ss5741934476	NC_000010.11:28877668:A:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
7690000379	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3689565071	NC_000010.11:28877672:A:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss39743806	NT_008705.16:29106616:A:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss39823288	NT_008705.16:29106616:AA:A	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4215309152	NC_000010.11:28877668::A	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
7690000379	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4215309153	NC_000010.11:28877668::AA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
7690000379	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4215309154	NC_000010.11:28877668::AAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3737188184	NC_000010.10:29166597::AAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4215309155	NC_000010.11:28877668::AAAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4215309156	NC_000010.11:28877668::AAAAAA	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3115146947	NC_000010.11:28877668:AAAAAAA:	NC_000010.11:28877668:AAAAAAAAAAAA… NC_000010.11:28877668:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA

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

No publications for rs35587006

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

rs35587006