Name: rs3051769
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.

rs3051769

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:35325412-35325426 (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)₄ / delAAA / delAA / delA / …
del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₆ / dup(A)₇ / dup(A)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.2316 (1160/5008, 1000G)
delAA=0.0000 (0/2088, ALFA)
delA=0.0000 (0/2088, ALFA) (+ 4 more)
dupA=0.0000 (0/2088, ALFA)
dupAA=0.0000 (0/2088, ALFA)
dupAAA=0.0000 (0/2088, ALFA)
dup(A)₄=0.0000 (0/2088, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC401324 : 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	2088	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	1264	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	530	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	14	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	516	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	42	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	38	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	26	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	142	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	6	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other	Sub	78	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	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
1000Genomes	Global	Study-wide	5008	(A)₁₅=0.7684	delA=0.2316
1000Genomes	African	Sub	1322	(A)₁₅=0.7829	delA=0.2171
1000Genomes	East Asian	Sub	1008	(A)₁₅=0.8770	delA=0.1230
1000Genomes	Europe	Sub	1006	(A)₁₅=0.7028	delA=0.2972
1000Genomes	South Asian	Sub	978	(A)₁₅=0.782	delA=0.218
1000Genomes	American	Sub	694	(A)₁₅=0.659	delA=0.341
Allele Frequency Aggregator	Total	Global	2088	(A)₁₅=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	1264	(A)₁₅=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	530	(A)₁₅=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	142	(A)₁₅=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	78	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Asian	Sub	42	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	26	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	6	(A)₁₅=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0

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 7	NC_000007.14:g.35325423_35325426del
GRCh38.p14 chr 7	NC_000007.14:g.35325424_35325426del
GRCh38.p14 chr 7	NC_000007.14:g.35325425_35325426del
GRCh38.p14 chr 7	NC_000007.14:g.35325426del
GRCh38.p14 chr 7	NC_000007.14:g.35325426dup
GRCh38.p14 chr 7	NC_000007.14:g.35325425_35325426dup
GRCh38.p14 chr 7	NC_000007.14:g.35325424_35325426dup
GRCh38.p14 chr 7	NC_000007.14:g.35325423_35325426dup
GRCh38.p14 chr 7	NC_000007.14:g.35325421_35325426dup
GRCh38.p14 chr 7	NC_000007.14:g.35325420_35325426dup
GRCh38.p14 chr 7	NC_000007.14:g.35325417_35325426dup
GRCh37.p13 chr 7	NC_000007.13:g.35365033_35365036del
GRCh37.p13 chr 7	NC_000007.13:g.35365034_35365036del
GRCh37.p13 chr 7	NC_000007.13:g.35365035_35365036del
GRCh37.p13 chr 7	NC_000007.13:g.35365036del
GRCh37.p13 chr 7	NC_000007.13:g.35365036dup
GRCh37.p13 chr 7	NC_000007.13:g.35365035_35365036dup
GRCh37.p13 chr 7	NC_000007.13:g.35365034_35365036dup
GRCh37.p13 chr 7	NC_000007.13:g.35365033_35365036dup
GRCh37.p13 chr 7	NC_000007.13:g.35365031_35365036dup
GRCh37.p13 chr 7	NC_000007.13:g.35365030_35365036dup
GRCh37.p13 chr 7	NC_000007.13:g.35365027_35365036dup

Gene: LOC401324, uncharacterized LOC401324 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC401324 transcript	NR_038864.1: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)₁₅=	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₆	dup(A)₇	dup(A)₁₀
GRCh38.p14 chr 7	NC_000007.14:g.35325412_35325426=	NC_000007.14:g.35325423_35325426del	NC_000007.14:g.35325424_35325426del	NC_000007.14:g.35325425_35325426del	NC_000007.14:g.35325426del	NC_000007.14:g.35325426dup	NC_000007.14:g.35325425_35325426dup	NC_000007.14:g.35325424_35325426dup	NC_000007.14:g.35325423_35325426dup	NC_000007.14:g.35325421_35325426dup	NC_000007.14:g.35325420_35325426dup	NC_000007.14:g.35325417_35325426dup
GRCh37.p13 chr 7	NC_000007.13:g.35365022_35365036=	NC_000007.13:g.35365033_35365036del	NC_000007.13:g.35365034_35365036del	NC_000007.13:g.35365035_35365036del	NC_000007.13:g.35365036del	NC_000007.13:g.35365036dup	NC_000007.13:g.35365035_35365036dup	NC_000007.13:g.35365034_35365036dup	NC_000007.13:g.35365033_35365036dup	NC_000007.13:g.35365031_35365036dup	NC_000007.13:g.35365030_35365036dup	NC_000007.13:g.35365027_35365036dup

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#.

59 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4283002	Mar 15, 2016 (147)
2	ABI	ss42924793	Mar 14, 2006 (126)
3	ABI	ss43106357	Mar 14, 2006 (137)
4	HGSV	ss80113893	Dec 04, 2013 (142)
5	HUMANGENOME_JCVI	ss98205815	Feb 13, 2009 (130)
6	GMI	ss288834030	May 04, 2012 (137)
7	PJP	ss295331319	May 09, 2011 (137)
8	BILGI_BIOE	ss666393502	Apr 25, 2013 (138)
9	1000GENOMES	ss1376954329	Aug 21, 2014 (142)
10	EVA_UK10K_ALSPAC	ss1705586063	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1705586140	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1710318769	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1710324083	Apr 01, 2015 (144)
14	SWEGEN	ss3000916144	Nov 17, 2017 (151)
15	EVA_DECODE	ss3719450270	Jul 13, 2019 (153)
16	EVA_DECODE	ss3719450271	Jul 13, 2019 (153)
17	EVA_DECODE	ss3719450272	Jul 13, 2019 (153)
18	EVA_DECODE	ss3719450273	Jul 13, 2019 (153)
19	EVA_DECODE	ss3719450274	Jul 13, 2019 (153)
20	ACPOP	ss3734519743	Jul 13, 2019 (153)
21	ACPOP	ss3734519744	Jul 13, 2019 (153)
22	PACBIO	ss3785782222	Jul 13, 2019 (153)
23	PACBIO	ss3791089603	Jul 13, 2019 (153)
24	PACBIO	ss3795969433	Jul 13, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3809573863	Jul 13, 2019 (153)
26	EVA	ss3830509121	Apr 26, 2020 (154)
27	EVA	ss3838742550	Apr 26, 2020 (154)
28	EVA	ss3844194197	Apr 26, 2020 (154)
29	KOGIC	ss3961223375	Apr 26, 2020 (154)
30	KOGIC	ss3961223376	Apr 26, 2020 (154)
31	KOGIC	ss3961223377	Apr 26, 2020 (154)
32	KOGIC	ss3961223378	Apr 26, 2020 (154)
33	GNOMAD	ss4161371440	Apr 26, 2021 (155)
34	GNOMAD	ss4161371441	Apr 26, 2021 (155)
35	GNOMAD	ss4161371442	Apr 26, 2021 (155)
36	GNOMAD	ss4161371443	Apr 26, 2021 (155)
37	GNOMAD	ss4161371444	Apr 26, 2021 (155)
38	GNOMAD	ss4161371445	Apr 26, 2021 (155)
39	GNOMAD	ss4161371446	Apr 26, 2021 (155)
40	GNOMAD	ss4161371447	Apr 26, 2021 (155)
41	GNOMAD	ss4161371448	Apr 26, 2021 (155)
42	GNOMAD	ss4161371449	Apr 26, 2021 (155)
43	GNOMAD	ss4161371450	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5182600569	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5182600570	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5182600571	Apr 26, 2021 (155)
47	1000G_HIGH_COVERAGE	ss5272449061	Oct 14, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5272449062	Oct 14, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5272449063	Oct 14, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5272449064	Oct 14, 2022 (156)
51	HUGCELL_USP	ss5469668538	Oct 14, 2022 (156)
52	HUGCELL_USP	ss5469668539	Oct 14, 2022 (156)
53	HUGCELL_USP	ss5469668540	Oct 14, 2022 (156)
54	HUGCELL_USP	ss5469668541	Oct 14, 2022 (156)
55	TOMMO_GENOMICS	ss5722276990	Oct 14, 2022 (156)
56	TOMMO_GENOMICS	ss5722276991	Oct 14, 2022 (156)
57	TOMMO_GENOMICS	ss5722276992	Oct 14, 2022 (156)
58	EVA	ss5822652804	Oct 14, 2022 (156)
59	EVA	ss5822652805	Oct 14, 2022 (156)
60	1000Genomes	NC_000007.13 - 35365022	Oct 12, 2018 (152)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 20401965 (NC_000007.13:35365021:A: 1051/3854) Row 20401966 (NC_000007.13:35365021::A 1217/3854)	-	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 20401965 (NC_000007.13:35365021:A: 1051/3854) Row 20401966 (NC_000007.13:35365021::A 1217/3854)	-	Oct 12, 2018 (152)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 257984468 (NC_000007.14:35325411::A 41761/113432) Row 257984469 (NC_000007.14:35325411::AA 176/113718) Row 257984470 (NC_000007.14:35325411::AAA 5/113770)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 257984468 (NC_000007.14:35325411::A 41761/113432) Row 257984469 (NC_000007.14:35325411::AA 176/113718) Row 257984470 (NC_000007.14:35325411::AAA 5/113770)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 257984468 (NC_000007.14:35325411::A 41761/113432) Row 257984469 (NC_000007.14:35325411::AA 176/113718) Row 257984470 (NC_000007.14:35325411::AAA 5/113770)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 257984468 (NC_000007.14:35325411::A 41761/113432) Row 257984469 (NC_000007.14:35325411::AA 176/113718) Row 257984470 (NC_000007.14:35325411::AAA 5/113770)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 257984468 (NC_000007.14:35325411::A 41761/113432) Row 257984469 (NC_000007.14:35325411::AA 176/113718) Row 257984470 (NC_000007.14:35325411::AAA 5/113770)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 257984468 (NC_000007.14:35325411::A 41761/113432) Row 257984469 (NC_000007.14:35325411::AA 176/113718) Row 257984470 (NC_000007.14:35325411::AAA 5/113770)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 257984468 (NC_000007.14:35325411::A 41761/113432) Row 257984469 (NC_000007.14:35325411::AA 176/113718) Row 257984470 (NC_000007.14:35325411::AAA 5/113770)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 257984468 (NC_000007.14:35325411::A 41761/113432) Row 257984469 (NC_000007.14:35325411::AA 176/113718) Row 257984470 (NC_000007.14:35325411::AAA 5/113770)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 257984468 (NC_000007.14:35325411::A 41761/113432) Row 257984469 (NC_000007.14:35325411::AA 176/113718) Row 257984470 (NC_000007.14:35325411::AAA 5/113770)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 257984468 (NC_000007.14:35325411::A 41761/113432) Row 257984469 (NC_000007.14:35325411::AA 176/113718) Row 257984470 (NC_000007.14:35325411::AAA 5/113770)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 257984468 (NC_000007.14:35325411::A 41761/113432) Row 257984469 (NC_000007.14:35325411::AA 176/113718) Row 257984470 (NC_000007.14:35325411::AAA 5/113770)...	-	Apr 26, 2021 (155)
74	Korean Genome Project Submission ignored due to conflicting rows: Row 17601376 (NC_000007.14:35325412:A: 259/1822) Row 17601377 (NC_000007.14:35325413::A 307/1822) Row 17601378 (NC_000007.14:35325411:AA: 10/1822)...	-	Apr 26, 2020 (154)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 17601376 (NC_000007.14:35325412:A: 259/1822) Row 17601377 (NC_000007.14:35325413::A 307/1822) Row 17601378 (NC_000007.14:35325411:AA: 10/1822)...	-	Apr 26, 2020 (154)
76	Korean Genome Project Submission ignored due to conflicting rows: Row 17601376 (NC_000007.14:35325412:A: 259/1822) Row 17601377 (NC_000007.14:35325413::A 307/1822) Row 17601378 (NC_000007.14:35325411:AA: 10/1822)...	-	Apr 26, 2020 (154)
77	Korean Genome Project Submission ignored due to conflicting rows: Row 17601376 (NC_000007.14:35325412:A: 259/1822) Row 17601377 (NC_000007.14:35325413::A 307/1822) Row 17601378 (NC_000007.14:35325411:AA: 10/1822)...	-	Apr 26, 2020 (154)
78	Northern Sweden Submission ignored due to conflicting rows: Row 7804608 (NC_000007.13:35365021:A: 142/468) Row 7804609 (NC_000007.13:35365021::A 80/468)	-	Jul 13, 2019 (153)
79	Northern Sweden Submission ignored due to conflicting rows: Row 7804608 (NC_000007.13:35365021:A: 142/468) Row 7804609 (NC_000007.13:35365021::A 80/468)	-	Jul 13, 2019 (153)
80	8.3KJPN Submission ignored due to conflicting rows: Row 40569876 (NC_000007.13:35365021:A: 2128/16754) Row 40569877 (NC_000007.13:35365021::A 2777/16754) Row 40569878 (NC_000007.13:35365021::AA 1/16754)	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 40569876 (NC_000007.13:35365021:A: 2128/16754) Row 40569877 (NC_000007.13:35365021::A 2777/16754) Row 40569878 (NC_000007.13:35365021::AA 1/16754)	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 40569876 (NC_000007.13:35365021:A: 2128/16754) Row 40569877 (NC_000007.13:35365021::A 2777/16754) Row 40569878 (NC_000007.13:35365021::AA 1/16754)	-	Apr 26, 2021 (155)
83	14KJPN Submission ignored due to conflicting rows: Row 56114094 (NC_000007.14:35325411::A 4802/28256) Row 56114095 (NC_000007.14:35325411:A: 3583/28256) Row 56114096 (NC_000007.14:35325411::AA 2/28256)	-	Oct 14, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 56114094 (NC_000007.14:35325411::A 4802/28256) Row 56114095 (NC_000007.14:35325411:A: 3583/28256) Row 56114096 (NC_000007.14:35325411::AA 2/28256)	-	Oct 14, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 56114094 (NC_000007.14:35325411::A 4802/28256) Row 56114095 (NC_000007.14:35325411:A: 3583/28256) Row 56114096 (NC_000007.14:35325411::AA 2/28256)	-	Oct 14, 2022 (156)
86	UK 10K study - Twins Submission ignored due to conflicting rows: Row 20401965 (NC_000007.13:35365021:A: 1026/3708) Row 20401966 (NC_000007.13:35365021::A 1172/3708)	-	Oct 12, 2018 (152)
87	UK 10K study - Twins Submission ignored due to conflicting rows: Row 20401965 (NC_000007.13:35365021:A: 1026/3708) Row 20401966 (NC_000007.13:35365021::A 1172/3708)	-	Oct 12, 2018 (152)
88	ALFA	NC_000007.14 - 35325412	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)
rs35288131	May 11, 2012 (137)
rs61679120	May 11, 2012 (137)
rs140698287	Sep 17, 2011 (135)
rs397943234	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4161371450	NC_000007.14:35325411:AAAA:	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3719450274, ss4161371449	NC_000007.14:35325411:AAA:	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3000916144	NC_000007.13:35365021:AA:	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3961223377, ss4161371448, ss5272449064, ss5469668541	NC_000007.14:35325411:AA:	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
6624071849	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3719450273	NC_000007.14:35325412:AA:	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss288834030	NC_000007.12:35331546:A:	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
36591827, ss1376954329, ss1705586063, ss1705586140, ss3734519743, ss3838742550, ss5182600569, ss5822652804	NC_000007.13:35365021:A:	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3809573863, ss3844194197, ss4161371447, ss5272449061, ss5469668538, ss5722276991	NC_000007.14:35325411:A:	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
6624071849	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3961223375	NC_000007.14:35325412:A:	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3719450272	NC_000007.14:35325413:A:	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss43106357	NT_007819.17:35355021:A:	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4283002	NT_007819.17:35355035:A:	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss295331319	NC_000007.12:35331561::A	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss666393502, ss3734519744, ss3785782222, ss3791089603, ss3795969433, ss3830509121, ss5182600570, ss5822652805	NC_000007.13:35365021::A	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss1710318769, ss1710324083	NC_000007.13:35365022::A	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4161371440, ss5272449062, ss5469668539, ss5722276990	NC_000007.14:35325411::A	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
6624071849	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3961223376	NC_000007.14:35325413::A	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3719450271	NC_000007.14:35325414::A	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss98205815	NT_007819.17:35355021::A	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss42924793	NT_007819.17:35355022::A	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4283002	NT_007819.17:35355035:A:AA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss80113893	NT_007819.17:35355036::A	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5182600571	NC_000007.13:35365021::AA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4161371441, ss5272449063, ss5469668540, ss5722276992	NC_000007.14:35325411::AA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
6624071849	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3961223378	NC_000007.14:35325413::AA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3719450270	NC_000007.14:35325414::AA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4161371442	NC_000007.14:35325411::AAA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
6624071849	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4161371443	NC_000007.14:35325411::AAAA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
6624071849	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4161371444	NC_000007.14:35325411::AAAAAA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4161371445	NC_000007.14:35325411::AAAAAAA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4161371446	NC_000007.14:35325411::AAAAAAAAAA	NC_000007.14:35325411:AAAAAAAAAAAA… NC_000007.14:35325411:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs3051769

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

rs3051769