Name: rs34437096
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.

rs34437096

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:70166827-70166844 (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)₇ / del(A)₆ / delAAA / delAA…
del(A)₇ / del(A)₆ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₆
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₇=0.0000 (0/3704, ALFA)
del(A)₆=0.0000 (0/3704, ALFA)
delAAA=0.0000 (0/3704, ALFA) (+ 6 more)
delAA=0.0000 (0/3704, ALFA)
delA=0.0000 (0/3704, ALFA)
dupA=0.0000 (0/3704, ALFA)
dupAA=0.0000 (0/3704, ALFA)
dupAAA=0.0000 (0/3704, ALFA)
dup(A)₆=0.0000 (0/3704, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SAR1A : 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	HWEP
Total	Global	3704	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2322	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	752	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	28	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	724	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	82	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	66	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	16	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	30	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	330	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	26	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	162	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	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	3704	(A)₁₈=1.0000	del(A)₇=0.0000, del(A)₆=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	European	Sub	2322	(A)₁₈=1.0000	del(A)₇=0.0000, del(A)₆=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	African	Sub	752	(A)₁₈=1.000	del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	330	(A)₁₈=1.000	del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Other	Sub	162	(A)₁₈=1.000	del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Asian	Sub	82	(A)₁₈=1.00	del(A)₇=0.00, del(A)₆=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	30	(A)₁₈=1.00	del(A)₇=0.00, del(A)₆=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	26	(A)₁₈=1.00	del(A)₇=0.00, del(A)₆=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₆=0.00

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.70166838_70166844del
GRCh38.p14 chr 10	NC_000010.11:g.70166839_70166844del
GRCh38.p14 chr 10	NC_000010.11:g.70166842_70166844del
GRCh38.p14 chr 10	NC_000010.11:g.70166843_70166844del
GRCh38.p14 chr 10	NC_000010.11:g.70166844del
GRCh38.p14 chr 10	NC_000010.11:g.70166844dup
GRCh38.p14 chr 10	NC_000010.11:g.70166843_70166844dup
GRCh38.p14 chr 10	NC_000010.11:g.70166842_70166844dup
GRCh38.p14 chr 10	NC_000010.11:g.70166841_70166844dup
GRCh38.p14 chr 10	NC_000010.11:g.70166839_70166844dup
GRCh37.p13 chr 10	NC_000010.10:g.71926594_71926600del
GRCh37.p13 chr 10	NC_000010.10:g.71926595_71926600del
GRCh37.p13 chr 10	NC_000010.10:g.71926598_71926600del
GRCh37.p13 chr 10	NC_000010.10:g.71926599_71926600del
GRCh37.p13 chr 10	NC_000010.10:g.71926600del
GRCh37.p13 chr 10	NC_000010.10:g.71926600dup
GRCh37.p13 chr 10	NC_000010.10:g.71926599_71926600dup
GRCh37.p13 chr 10	NC_000010.10:g.71926598_71926600dup
GRCh37.p13 chr 10	NC_000010.10:g.71926597_71926600dup
GRCh37.p13 chr 10	NC_000010.10:g.71926595_71926600dup

Gene: SAR1A, secretion associated Ras related GTPase 1A (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SAR1A transcript variant 1	NM_001142648.2:c.-87+3580… NM_001142648.2:c.-87+3580_-87+3586del	N/A	Intron Variant
SAR1A transcript variant 2	NM_020150.5:c.-17+3580_-1… NM_020150.5:c.-17+3580_-17+3586del	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)₁₈=	del(A)₇	del(A)₆	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₆
GRCh38.p14 chr 10	NC_000010.11:g.70166827_70166844=	NC_000010.11:g.70166838_70166844del	NC_000010.11:g.70166839_70166844del	NC_000010.11:g.70166842_70166844del	NC_000010.11:g.70166843_70166844del	NC_000010.11:g.70166844del	NC_000010.11:g.70166844dup	NC_000010.11:g.70166843_70166844dup	NC_000010.11:g.70166842_70166844dup	NC_000010.11:g.70166841_70166844dup	NC_000010.11:g.70166839_70166844dup
GRCh37.p13 chr 10	NC_000010.10:g.71926583_71926600=	NC_000010.10:g.71926594_71926600del	NC_000010.10:g.71926595_71926600del	NC_000010.10:g.71926598_71926600del	NC_000010.10:g.71926599_71926600del	NC_000010.10:g.71926600del	NC_000010.10:g.71926600dup	NC_000010.10:g.71926599_71926600dup	NC_000010.10:g.71926598_71926600dup	NC_000010.10:g.71926597_71926600dup	NC_000010.10:g.71926595_71926600dup
SAR1A transcript variant 1	NM_001142648.1:c.-87+3586=	NM_001142648.1:c.-87+3580_-87+3586del	NM_001142648.1:c.-87+3581_-87+3586del	NM_001142648.1:c.-87+3584_-87+3586del	NM_001142648.1:c.-87+3585_-87+3586del	NM_001142648.1:c.-87+3586del	NM_001142648.1:c.-87+3586dup	NM_001142648.1:c.-87+3585_-87+3586dup	NM_001142648.1:c.-87+3584_-87+3586dup	NM_001142648.1:c.-87+3583_-87+3586dup	NM_001142648.1:c.-87+3581_-87+3586dup
SAR1A transcript variant 1	NM_001142648.2:c.-87+3586=	NM_001142648.2:c.-87+3580_-87+3586del	NM_001142648.2:c.-87+3581_-87+3586del	NM_001142648.2:c.-87+3584_-87+3586del	NM_001142648.2:c.-87+3585_-87+3586del	NM_001142648.2:c.-87+3586del	NM_001142648.2:c.-87+3586dup	NM_001142648.2:c.-87+3585_-87+3586dup	NM_001142648.2:c.-87+3584_-87+3586dup	NM_001142648.2:c.-87+3583_-87+3586dup	NM_001142648.2:c.-87+3581_-87+3586dup
SAR1A transcript variant 2	NM_020150.4:c.-17+3586=	NM_020150.4:c.-17+3580_-17+3586del	NM_020150.4:c.-17+3581_-17+3586del	NM_020150.4:c.-17+3584_-17+3586del	NM_020150.4:c.-17+3585_-17+3586del	NM_020150.4:c.-17+3586del	NM_020150.4:c.-17+3586dup	NM_020150.4:c.-17+3585_-17+3586dup	NM_020150.4:c.-17+3584_-17+3586dup	NM_020150.4:c.-17+3583_-17+3586dup	NM_020150.4:c.-17+3581_-17+3586dup
SAR1A transcript variant 2	NM_020150.5:c.-17+3586=	NM_020150.5:c.-17+3580_-17+3586del	NM_020150.5:c.-17+3581_-17+3586del	NM_020150.5:c.-17+3584_-17+3586del	NM_020150.5:c.-17+3585_-17+3586del	NM_020150.5:c.-17+3586del	NM_020150.5:c.-17+3586dup	NM_020150.5:c.-17+3585_-17+3586dup	NM_020150.5:c.-17+3584_-17+3586dup	NM_020150.5:c.-17+3583_-17+3586dup	NM_020150.5:c.-17+3581_-17+3586dup
SAR1A transcript variant X1	XM_005269984.1:c.-17+3649=	XM_005269984.1:c.-17+3643_-17+3649del	XM_005269984.1:c.-17+3644_-17+3649del	XM_005269984.1:c.-17+3647_-17+3649del	XM_005269984.1:c.-17+3648_-17+3649del	XM_005269984.1:c.-17+3649del	XM_005269984.1:c.-17+3649dup	XM_005269984.1:c.-17+3648_-17+3649dup	XM_005269984.1:c.-17+3647_-17+3649dup	XM_005269984.1:c.-17+3646_-17+3649dup	XM_005269984.1:c.-17+3644_-17+3649dup

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#.

49 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss39844191	Mar 13, 2006 (126)
2	HGSV	ss83900186	Dec 05, 2013 (144)
3	HUMANGENOME_JCVI	ss95545157	Feb 04, 2009 (130)
4	PJP	ss294663022	May 09, 2011 (137)
5	PJP	ss294663023	May 09, 2011 (135)
6	SSIP	ss947260883	Aug 21, 2014 (142)
7	SWEGEN	ss3006684181	Nov 08, 2017 (151)
8	EVA_DECODE	ss3690127895	Jul 13, 2019 (153)
9	EVA_DECODE	ss3690127896	Jul 13, 2019 (153)
10	EVA_DECODE	ss3690127897	Jul 13, 2019 (153)
11	EVA_DECODE	ss3690127898	Jul 13, 2019 (153)
12	PACBIO	ss3786709579	Jul 13, 2019 (153)
13	PACBIO	ss3791885140	Jul 13, 2019 (153)
14	PACBIO	ss3796767164	Jul 13, 2019 (153)
15	EVA	ss3832191940	Apr 26, 2020 (154)
16	GNOMAD	ss4220680469	Apr 26, 2021 (155)
17	GNOMAD	ss4220680470	Apr 26, 2021 (155)
18	GNOMAD	ss4220680471	Apr 26, 2021 (155)
19	GNOMAD	ss4220680472	Apr 26, 2021 (155)
20	GNOMAD	ss4220680473	Apr 26, 2021 (155)
21	GNOMAD	ss4220680475	Apr 26, 2021 (155)
22	GNOMAD	ss4220680476	Apr 26, 2021 (155)
23	GNOMAD	ss4220680477	Apr 26, 2021 (155)
24	GNOMAD	ss4220680478	Apr 26, 2021 (155)
25	TOPMED	ss4856702681	Apr 26, 2021 (155)
26	TOPMED	ss4856702682	Apr 26, 2021 (155)
27	TOPMED	ss4856702683	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5198191024	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5198191025	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5198191026	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5198191027	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5198191028	Apr 26, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5284487710	Oct 16, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5284487711	Oct 16, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5284487712	Oct 16, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5284487713	Oct 16, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5284487714	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5480021717	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5480021718	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5480021719	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5480021720	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5744182716	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5744182717	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5744182718	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5744182719	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5744182721	Oct 16, 2022 (156)
47	EVA	ss5824571726	Oct 16, 2022 (156)
48	EVA	ss5824571727	Oct 16, 2022 (156)
49	EVA	ss5849622673	Oct 16, 2022 (156)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355796134 (NC_000010.11:70166826::A 44000/92464) Row 355796135 (NC_000010.11:70166826::AA 197/92582) Row 355796136 (NC_000010.11:70166826::AAA 130/92596)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355796134 (NC_000010.11:70166826::A 44000/92464) Row 355796135 (NC_000010.11:70166826::AA 197/92582) Row 355796136 (NC_000010.11:70166826::AAA 130/92596)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355796134 (NC_000010.11:70166826::A 44000/92464) Row 355796135 (NC_000010.11:70166826::AA 197/92582) Row 355796136 (NC_000010.11:70166826::AAA 130/92596)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355796134 (NC_000010.11:70166826::A 44000/92464) Row 355796135 (NC_000010.11:70166826::AA 197/92582) Row 355796136 (NC_000010.11:70166826::AAA 130/92596)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355796134 (NC_000010.11:70166826::A 44000/92464) Row 355796135 (NC_000010.11:70166826::AA 197/92582) Row 355796136 (NC_000010.11:70166826::AAA 130/92596)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355796134 (NC_000010.11:70166826::A 44000/92464) Row 355796135 (NC_000010.11:70166826::AA 197/92582) Row 355796136 (NC_000010.11:70166826::AAA 130/92596)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355796134 (NC_000010.11:70166826::A 44000/92464) Row 355796135 (NC_000010.11:70166826::AA 197/92582) Row 355796136 (NC_000010.11:70166826::AAA 130/92596)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355796134 (NC_000010.11:70166826::A 44000/92464) Row 355796135 (NC_000010.11:70166826::AA 197/92582) Row 355796136 (NC_000010.11:70166826::AAA 130/92596)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355796134 (NC_000010.11:70166826::A 44000/92464) Row 355796135 (NC_000010.11:70166826::AA 197/92582) Row 355796136 (NC_000010.11:70166826::AAA 130/92596)...	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 56160331 (NC_000010.10:71926582:AA: 1190/16754) Row 56160332 (NC_000010.10:71926582:A: 51/16754) Row 56160333 (NC_000010.10:71926582::A 365/16754)...	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 56160331 (NC_000010.10:71926582:AA: 1190/16754) Row 56160332 (NC_000010.10:71926582:A: 51/16754) Row 56160333 (NC_000010.10:71926582::A 365/16754)...	-	Apr 26, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 56160331 (NC_000010.10:71926582:AA: 1190/16754) Row 56160332 (NC_000010.10:71926582:A: 51/16754) Row 56160333 (NC_000010.10:71926582::A 365/16754)...	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 56160331 (NC_000010.10:71926582:AA: 1190/16754) Row 56160332 (NC_000010.10:71926582:A: 51/16754) Row 56160333 (NC_000010.10:71926582::A 365/16754)...	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 56160331 (NC_000010.10:71926582:AA: 1190/16754) Row 56160332 (NC_000010.10:71926582:A: 51/16754) Row 56160333 (NC_000010.10:71926582::A 365/16754)...	-	Apr 26, 2021 (155)
64	14KJPN Submission ignored due to conflicting rows: Row 78019820 (NC_000010.11:70166826:A: 61/28252) Row 78019821 (NC_000010.11:70166826::A 612/28252) Row 78019822 (NC_000010.11:70166826:AA: 1973/28252)...	-	Oct 16, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 78019820 (NC_000010.11:70166826:A: 61/28252) Row 78019821 (NC_000010.11:70166826::A 612/28252) Row 78019822 (NC_000010.11:70166826:AA: 1973/28252)...	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 78019820 (NC_000010.11:70166826:A: 61/28252) Row 78019821 (NC_000010.11:70166826::A 612/28252) Row 78019822 (NC_000010.11:70166826:AA: 1973/28252)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 78019820 (NC_000010.11:70166826:A: 61/28252) Row 78019821 (NC_000010.11:70166826::A 612/28252) Row 78019822 (NC_000010.11:70166826:AA: 1973/28252)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 78019820 (NC_000010.11:70166826:A: 61/28252) Row 78019821 (NC_000010.11:70166826::A 612/28252) Row 78019822 (NC_000010.11:70166826:AA: 1973/28252)...	-	Oct 16, 2022 (156)
69	TopMed Submission ignored due to conflicting rows: Row 72248336 (NC_000010.11:70166826:AA: 8751/264690) Row 72248337 (NC_000010.11:70166826:AAAAAA: 1/264690) Row 72248338 (NC_000010.11:70166826:AAAAAAA: 1/264690)	-	Apr 26, 2021 (155)
70	TopMed Submission ignored due to conflicting rows: Row 72248336 (NC_000010.11:70166826:AA: 8751/264690) Row 72248337 (NC_000010.11:70166826:AAAAAA: 1/264690) Row 72248338 (NC_000010.11:70166826:AAAAAAA: 1/264690)	-	Apr 26, 2021 (155)
71	TopMed Submission ignored due to conflicting rows: Row 72248336 (NC_000010.11:70166826:AA: 8751/264690) Row 72248337 (NC_000010.11:70166826:AAAAAA: 1/264690) Row 72248338 (NC_000010.11:70166826:AAAAAAA: 1/264690)	-	Apr 26, 2021 (155)
72	ALFA	NC_000010.11 - 70166827	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)
rs59969081	May 23, 2008 (130)
rs67470447	May 11, 2012 (137)
rs67470448	Feb 27, 2009 (130)
rs142348780	Sep 17, 2011 (135)
rs148732554	Sep 17, 2011 (135)
rs397978405	Jul 01, 2015 (144)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5198191028	NC_000010.10:71926582:AAAAAAA:	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4220680478, ss4856702683, ss5744182721	NC_000010.11:70166826:AAAAAAA:	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
12596917784	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4856702682	NC_000010.11:70166826:AAAAAA:	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
12596917784	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4220680477	NC_000010.11:70166826:AAA:	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
12596917784	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3006684181, ss5198191024	NC_000010.10:71926582:AA:	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3690127898, ss4220680476, ss4856702681, ss5284487712, ss5480021720, ss5744182718	NC_000010.11:70166826:AA:	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
12596917784	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5198191025	NC_000010.10:71926582:A:	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4220680475, ss5284487710, ss5480021718, ss5744182716, ss5849622673	NC_000010.11:70166826:A:	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
12596917784	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3690127897	NC_000010.11:70166827:A:	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss294663022	NC_000010.9:71596589::A	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss294663023	NC_000010.9:71596606::A	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3786709579, ss3791885140, ss3796767164, ss3832191940, ss5198191026, ss5824571726	NC_000010.10:71926582::A	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss947260883	NC_000010.10:71926583::A	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4220680469, ss5284487711, ss5480021717, ss5744182717	NC_000010.11:70166826::A	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
12596917784	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3690127896	NC_000010.11:70166828::A	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss39844191, ss83900186, ss95545157	NT_030059.13:22731064::A	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5198191027, ss5824571727	NC_000010.10:71926582::AA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4220680470, ss5284487713, ss5480021719, ss5744182719	NC_000010.11:70166826::AA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
12596917784	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3690127895	NC_000010.11:70166828::AA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4220680471, ss5284487714	NC_000010.11:70166826::AAA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
12596917784	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4220680472	NC_000010.11:70166826::AAAA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220680473	NC_000010.11:70166826::AAAAAA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
12596917784	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:70166826:AAAAAAAAAAAA… NC_000010.11:70166826:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(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 rs34437096

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

rs34437096