Name: rs35450922
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.

rs35450922

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:21237594-21237607 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.0622 (397/6382, ALFA)
dupA=0.2145 (1074/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ANKS4B : 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	6382	AAAAAAAAAAAAAA=0.9378	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0622, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	0.883109	0.007521	0.10937	7
European	Sub	4798	AAAAAAAAAAAAAA=0.9193	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0807, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	0.848687	0.010004	0.141309	3
African	Sub	1178	AAAAAAAAAAAAAA=0.9949	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0051, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	0.989813	0.0	0.010187	0
African Others	Sub	50	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1128	AAAAAAAAAAAAAA=0.9947	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0053, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	0.989362	0.0	0.010638	0
Asian	Sub	36	AAAAAAAAAAAAAA=0.97	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.03, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	0.944444	0.0	0.055556	0
East Asian	Sub	28	AAAAAAAAAAAAAA=0.96	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.04, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	0.928571	0.0	0.071429	0
Other Asian	Sub	8	AAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	50	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	122	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	26	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	172	AAAAAAAAAAAAAA=0.983	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.017, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	0.965116	0.0	0.034884	0

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	6382	(A)₁₄=0.9378	delAA=0.0000, delA=0.0622, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	4798	(A)₁₄=0.9193	delAA=0.0000, delA=0.0807, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	1178	(A)₁₄=0.9949	delAA=0.0000, delA=0.0051, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	Other	Sub	172	(A)₁₄=0.983	delAA=0.000, delA=0.017, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	122	(A)₁₄=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	50	(A)₁₄=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	36	(A)₁₄=0.97	delAA=0.00, delA=0.03, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	26	(A)₁₄=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupA=0.2145
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.2133
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.2014
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.1809
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.258
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.223

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 16	NC_000016.10:g.21237605_21237607del
GRCh38.p14 chr 16	NC_000016.10:g.21237606_21237607del
GRCh38.p14 chr 16	NC_000016.10:g.21237607del
GRCh38.p14 chr 16	NC_000016.10:g.21237607dup
GRCh38.p14 chr 16	NC_000016.10:g.21237606_21237607dup
GRCh38.p14 chr 16	NC_000016.10:g.21237605_21237607dup
GRCh38.p14 chr 16	NC_000016.10:g.21237604_21237607dup
GRCh37.p13 chr 16	NC_000016.9:g.21248926_21248928del
GRCh37.p13 chr 16	NC_000016.9:g.21248927_21248928del
GRCh37.p13 chr 16	NC_000016.9:g.21248928del
GRCh37.p13 chr 16	NC_000016.9:g.21248928dup
GRCh37.p13 chr 16	NC_000016.9:g.21248927_21248928dup
GRCh37.p13 chr 16	NC_000016.9:g.21248926_21248928dup
GRCh37.p13 chr 16	NC_000016.9:g.21248925_21248928dup
GRCh38.p14 chr 16 fix patch HG926_PATCH	NW_017852933.1:g.61296_61298del
GRCh38.p14 chr 16 fix patch HG926_PATCH	NW_017852933.1:g.61297_61298del
GRCh38.p14 chr 16 fix patch HG926_PATCH	NW_017852933.1:g.61298del
GRCh38.p14 chr 16 fix patch HG926_PATCH	NW_017852933.1:g.61298dup
GRCh38.p14 chr 16 fix patch HG926_PATCH	NW_017852933.1:g.61297_61298dup
GRCh38.p14 chr 16 fix patch HG926_PATCH	NW_017852933.1:g.61296_61298dup
GRCh38.p14 chr 16 fix patch HG926_PATCH	NW_017852933.1:g.61295_61298dup

Gene: ANKS4B, ankyrin repeat and sterile alpha motif domain containing 4B (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ANKS4B transcript	NM_145865.3:c.164+3704_16… NM_145865.3:c.164+3704_164+3706del	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)₁₄=	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄
GRCh38.p14 chr 16	NC_000016.10:g.21237594_21237607=	NC_000016.10:g.21237605_21237607del	NC_000016.10:g.21237606_21237607del	NC_000016.10:g.21237607del	NC_000016.10:g.21237607dup	NC_000016.10:g.21237606_21237607dup	NC_000016.10:g.21237605_21237607dup	NC_000016.10:g.21237604_21237607dup
GRCh37.p13 chr 16	NC_000016.9:g.21248915_21248928=	NC_000016.9:g.21248926_21248928del	NC_000016.9:g.21248927_21248928del	NC_000016.9:g.21248928del	NC_000016.9:g.21248928dup	NC_000016.9:g.21248927_21248928dup	NC_000016.9:g.21248926_21248928dup	NC_000016.9:g.21248925_21248928dup
GRCh38.p14 chr 16 fix patch HG926_PATCH	NW_017852933.1:g.61285_61298=	NW_017852933.1:g.61296_61298del	NW_017852933.1:g.61297_61298del	NW_017852933.1:g.61298del	NW_017852933.1:g.61298dup	NW_017852933.1:g.61297_61298dup	NW_017852933.1:g.61296_61298dup	NW_017852933.1:g.61295_61298dup
ANKS4B transcript	NM_145865.2:c.164+3693=	NM_145865.2:c.164+3704_164+3706del	NM_145865.2:c.164+3705_164+3706del	NM_145865.2:c.164+3706del	NM_145865.2:c.164+3706dup	NM_145865.2:c.164+3705_164+3706dup	NM_145865.2:c.164+3704_164+3706dup	NM_145865.2:c.164+3703_164+3706dup
ANKS4B transcript	NM_145865.3:c.164+3693=	NM_145865.3:c.164+3704_164+3706del	NM_145865.3:c.164+3705_164+3706del	NM_145865.3:c.164+3706del	NM_145865.3:c.164+3706dup	NM_145865.3:c.164+3705_164+3706dup	NM_145865.3:c.164+3704_164+3706dup	NM_145865.3:c.164+3703_164+3706dup

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#.

55 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40643054	Dec 03, 2013 (142)
2	ABI	ss40688337	Mar 15, 2006 (126)
3	HUMANGENOME_JCVI	ss95674341	Dec 05, 2013 (138)
4	BCMHGSC_JDW	ss103584782	Dec 01, 2009 (131)
5	BUSHMAN	ss193411079	Jul 04, 2010 (132)
6	GMI	ss289287481	May 04, 2012 (137)
7	GMI	ss289287482	May 04, 2012 (138)
8	SSMP	ss664305964	Apr 01, 2015 (144)
9	1000GENOMES	ss1375659609	Aug 21, 2014 (142)
10	EVA_UK10K_ALSPAC	ss1708498135	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1708498495	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1710694461	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1710694466	Apr 01, 2015 (144)
14	HAMMER_LAB	ss1808461551	Sep 08, 2015 (146)
15	SWEGEN	ss3014219118	Nov 08, 2017 (151)
16	URBANLAB	ss3650484800	Oct 12, 2018 (152)
17	EVA_DECODE	ss3699007425	Jul 13, 2019 (153)
18	EVA_DECODE	ss3699007426	Jul 13, 2019 (153)
19	EVA_DECODE	ss3699007427	Jul 13, 2019 (153)
20	EVA_DECODE	ss3699007428	Jul 13, 2019 (153)
21	EVA_DECODE	ss3699007429	Jul 13, 2019 (153)
22	PACBIO	ss3788004862	Jul 13, 2019 (153)
23	PACBIO	ss3788004863	Jul 13, 2019 (153)
24	PACBIO	ss3792994751	Jul 13, 2019 (153)
25	PACBIO	ss3792994752	Jul 13, 2019 (153)
26	PACBIO	ss3797879704	Jul 13, 2019 (153)
27	PACBIO	ss3797879705	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3819083343	Jul 13, 2019 (153)
29	EVA	ss3834516996	Apr 27, 2020 (154)
30	EVA	ss3846356788	Apr 27, 2020 (154)
31	KOGIC	ss3977261226	Apr 27, 2020 (154)
32	KOGIC	ss3977261227	Apr 27, 2020 (154)
33	KOGIC	ss3977261228	Apr 27, 2020 (154)
34	GNOMAD	ss4298352100	Apr 27, 2021 (155)
35	GNOMAD	ss4298352101	Apr 27, 2021 (155)
36	GNOMAD	ss4298352102	Apr 27, 2021 (155)
37	GNOMAD	ss4298352103	Apr 27, 2021 (155)
38	GNOMAD	ss4298352104	Apr 27, 2021 (155)
39	GNOMAD	ss4298352105	Apr 27, 2021 (155)
40	GNOMAD	ss4298352106	Apr 27, 2021 (155)
41	TOMMO_GENOMICS	ss5218850400	Apr 27, 2021 (155)
42	TOMMO_GENOMICS	ss5218850401	Apr 27, 2021 (155)
43	TOMMO_GENOMICS	ss5218850402	Apr 27, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5300449281	Oct 17, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5300449282	Oct 17, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5300449283	Oct 17, 2022 (156)
47	HUGCELL_USP	ss5493919171	Oct 17, 2022 (156)
48	HUGCELL_USP	ss5493919172	Oct 17, 2022 (156)
49	HUGCELL_USP	ss5493919173	Oct 17, 2022 (156)
50	TOMMO_GENOMICS	ss5773453936	Oct 17, 2022 (156)
51	TOMMO_GENOMICS	ss5773453937	Oct 17, 2022 (156)
52	TOMMO_GENOMICS	ss5773453939	Oct 17, 2022 (156)
53	EVA	ss5846223894	Oct 17, 2022 (156)
54	EVA	ss5846223895	Oct 17, 2022 (156)
55	EVA	ss5898606560	Oct 17, 2022 (156)
56	1000Genomes	NC_000016.9 - 21248915	Oct 12, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 38232282 (NC_000016.9:21248914::A 805/3854) Row 38232283 (NC_000016.9:21248914:A: 760/3854)	-	Oct 12, 2018 (152)
58	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 38232282 (NC_000016.9:21248914::A 805/3854) Row 38232283 (NC_000016.9:21248914:A: 760/3854)	-	Oct 12, 2018 (152)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485337191 (NC_000016.10:21237593::A 33836/114822) Row 485337192 (NC_000016.10:21237593::AA 195/115016) Row 485337193 (NC_000016.10:21237593::AAA 3/115054)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485337191 (NC_000016.10:21237593::A 33836/114822) Row 485337192 (NC_000016.10:21237593::AA 195/115016) Row 485337193 (NC_000016.10:21237593::AAA 3/115054)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485337191 (NC_000016.10:21237593::A 33836/114822) Row 485337192 (NC_000016.10:21237593::AA 195/115016) Row 485337193 (NC_000016.10:21237593::AAA 3/115054)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485337191 (NC_000016.10:21237593::A 33836/114822) Row 485337192 (NC_000016.10:21237593::AA 195/115016) Row 485337193 (NC_000016.10:21237593::AAA 3/115054)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485337191 (NC_000016.10:21237593::A 33836/114822) Row 485337192 (NC_000016.10:21237593::AA 195/115016) Row 485337193 (NC_000016.10:21237593::AAA 3/115054)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485337191 (NC_000016.10:21237593::A 33836/114822) Row 485337192 (NC_000016.10:21237593::AA 195/115016) Row 485337193 (NC_000016.10:21237593::AAA 3/115054)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485337191 (NC_000016.10:21237593::A 33836/114822) Row 485337192 (NC_000016.10:21237593::AA 195/115016) Row 485337193 (NC_000016.10:21237593::AAA 3/115054)...	-	Apr 27, 2021 (155)
66	Korean Genome Project Submission ignored due to conflicting rows: Row 33639227 (NC_000016.10:21237593:A: 152/1830) Row 33639228 (NC_000016.10:21237594::A 605/1830) Row 33639229 (NC_000016.10:21237594::AA 21/1830)	-	Apr 27, 2020 (154)
67	Korean Genome Project Submission ignored due to conflicting rows: Row 33639227 (NC_000016.10:21237593:A: 152/1830) Row 33639228 (NC_000016.10:21237594::A 605/1830) Row 33639229 (NC_000016.10:21237594::AA 21/1830)	-	Apr 27, 2020 (154)
68	Korean Genome Project Submission ignored due to conflicting rows: Row 33639227 (NC_000016.10:21237593:A: 152/1830) Row 33639228 (NC_000016.10:21237594::A 605/1830) Row 33639229 (NC_000016.10:21237594::AA 21/1830)	-	Apr 27, 2020 (154)
69	8.3KJPN Submission ignored due to conflicting rows: Row 76819707 (NC_000016.9:21248914::A 5983/16754) Row 76819708 (NC_000016.9:21248914:A: 655/16754) Row 76819709 (NC_000016.9:21248914::AA 17/16754)	-	Apr 27, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 76819707 (NC_000016.9:21248914::A 5983/16754) Row 76819708 (NC_000016.9:21248914:A: 655/16754) Row 76819709 (NC_000016.9:21248914::AA 17/16754)	-	Apr 27, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 76819707 (NC_000016.9:21248914::A 5983/16754) Row 76819708 (NC_000016.9:21248914:A: 655/16754) Row 76819709 (NC_000016.9:21248914::AA 17/16754)	-	Apr 27, 2021 (155)
72	14KJPN Submission ignored due to conflicting rows: Row 107291040 (NC_000016.10:21237593::A 10064/28258) Row 107291041 (NC_000016.10:21237593:A: 1127/28258) Row 107291043 (NC_000016.10:21237593::AA 26/28258)	-	Oct 17, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 107291040 (NC_000016.10:21237593::A 10064/28258) Row 107291041 (NC_000016.10:21237593:A: 1127/28258) Row 107291043 (NC_000016.10:21237593::AA 26/28258)	-	Oct 17, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 107291040 (NC_000016.10:21237593::A 10064/28258) Row 107291041 (NC_000016.10:21237593:A: 1127/28258) Row 107291043 (NC_000016.10:21237593::AA 26/28258)	-	Oct 17, 2022 (156)
75	UK 10K study - Twins Submission ignored due to conflicting rows: Row 38232282 (NC_000016.9:21248914::A 768/3708) Row 38232283 (NC_000016.9:21248914:A: 716/3708)	-	Oct 12, 2018 (152)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 38232282 (NC_000016.9:21248914::A 768/3708) Row 38232283 (NC_000016.9:21248914:A: 716/3708)	-	Oct 12, 2018 (152)
77	ALFA	NC_000016.10 - 21237594	Apr 27, 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)
rs71151625	May 11, 2012 (137)
rs201986772	May 15, 2013 (138)
rs397854616	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3699007429, ss4298352106	NC_000016.10:21237593:AAA:	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss103584782	NT_010393.16:21188925:AAA:	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4298352105	NC_000016.10:21237593:AA:	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
2181709920	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3699007428	NC_000016.10:21237594:AA:	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss289287481	NC_000016.8:21156415:A:	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1708498135, ss1708498495, ss3014219118, ss3788004862, ss3792994751, ss3797879704, ss5218850401, ss5846223894	NC_000016.9:21248914:A:	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3650484800, ss3846356788, ss3977261226, ss4298352104, ss5300449281, ss5493919171, ss5773453937	NC_000016.10:21237593:A:	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
2181709920	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3699007427	NC_000016.10:21237595:A:	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss40688337	NT_010393.16:21188914:A:	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss95674341	NT_010393.16:21188927:A:	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss289287482	NC_000016.8:21156429::A	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
68870496, ss664305964, ss1375659609, ss1808461551, ss3788004863, ss3792994752, ss3797879705, ss3834516996, ss5218850400, ss5846223895	NC_000016.9:21248914::A	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss1710694461, ss1710694466	NC_000016.9:21248915::A	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3819083343, ss4298352100, ss5300449282, ss5493919172, ss5773453936, ss5898606560	NC_000016.10:21237593::A	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
2181709920	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3977261227	NC_000016.10:21237594::A	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3699007426	NC_000016.10:21237596::A	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss40643054	NT_010393.16:21188915::A	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss193411079	NT_187260.1:2751107::A	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5218850402	NC_000016.9:21248914::AA	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4298352101, ss5300449283, ss5493919173, ss5773453939	NC_000016.10:21237593::AA	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
2181709920	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3977261228	NC_000016.10:21237594::AA	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3699007425	NC_000016.10:21237596::AA	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4298352102	NC_000016.10:21237593::AAA	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
2181709920	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4298352103	NC_000016.10:21237593::AAAA	NC_000016.10:21237593:AAAAAAAAAAAA… NC_000016.10:21237593:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(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 rs35450922

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

rs35450922