Name: rs35869936
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.

rs35869936

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:38919002-38919020 (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: delCACA / delCA / dupCA / dupCACA …
delCACA / delCA / dupCA / dupCACA / dup(CA)₃
Variation Type: Indel Insertion and Deletion
Frequency: dup(CA)₃=0.000246 (65/264690, TOPMED)
dupCA=0.04926 (702/14252, ALFA)
dupCA=0.2408 (1206/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PPP1R16B : 3 Prime UTR 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	14252	ACACACACACACACACACA=0.95018	ACACACACACACACACA=0.00000, ACACACACACACACACACACA=0.04926, ACACACACACACACACACACACA=0.00056, ACACACACACACACACACACACACA=0.00000	0.907558	0.006041	0.086401	23
European	Sub	11412	ACACACACACACACACACA=0.93805	ACACACACACACACACA=0.00000, ACACACACACACACACACACA=0.06125, ACACACACACACACACACACACA=0.00070, ACACACACACACACACACACACACA=0.00000	0.885047	0.007547	0.107406	14
African	Sub	1916	ACACACACACACACACACA=1.0000	ACACACACACACACACA=0.0000, ACACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	74	ACACACACACACACACACA=1.00	ACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1842	ACACACACACACACACACA=1.0000	ACACACACACACACACA=0.0000, ACACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	52	ACACACACACACACACACA=1.00	ACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	42	ACACACACACACACACACA=1.00	ACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	ACACACACACACACACACA=1.0	ACACACACACACACACA=0.0, ACACACACACACACACACACA=0.0, ACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	94	ACACACACACACACACACA=1.00	ACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	366	ACACACACACACACACACA=1.000	ACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	70	ACACACACACACACACACA=1.00	ACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other	Sub	342	ACACACACACACACACACA=0.991	ACACACACACACACACA=0.000, ACACACACACACACACACACA=0.009, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000	0.982456	0.0	0.017544	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	- No frequency provided	dup(CA)₃=0.000246
Allele Frequency Aggregator	Total	Global	14252	(AC)₉A=0.95018	delCA=0.00000, dupCA=0.04926, dupCACA=0.00056, dup(CA)₃=0.00000
Allele Frequency Aggregator	European	Sub	11412	(AC)₉A=0.93805	delCA=0.00000, dupCA=0.06125, dupCACA=0.00070, dup(CA)₃=0.00000
Allele Frequency Aggregator	African	Sub	1916	(AC)₉A=1.0000	delCA=0.0000, dupCA=0.0000, dupCACA=0.0000, dup(CA)₃=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	366	(AC)₉A=1.000	delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000
Allele Frequency Aggregator	Other	Sub	342	(AC)₉A=0.991	delCA=0.000, dupCA=0.009, dupCACA=0.000, dup(CA)₃=0.000
Allele Frequency Aggregator	Latin American 1	Sub	94	(AC)₉A=1.00	delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00
Allele Frequency Aggregator	South Asian	Sub	70	(AC)₉A=1.00	delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00
Allele Frequency Aggregator	Asian	Sub	52	(AC)₉A=1.00	delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupCA=0.2408
1000Genomes	African	Sub	1322	- No frequency provided	dupCA=0.2148
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupCA=0.3175
1000Genomes	Europe	Sub	1006	- No frequency provided	dupCA=0.2078
1000Genomes	South Asian	Sub	978	- No frequency provided	dupCA=0.213
1000Genomes	American	Sub	694	- No frequency provided	dupCA=0.267

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 20	NC_000020.11:g.38919003CA[7]
GRCh38.p14 chr 20	NC_000020.11:g.38919003CA[8]
GRCh38.p14 chr 20	NC_000020.11:g.38919003CA[10]
GRCh38.p14 chr 20	NC_000020.11:g.38919003CA[11]
GRCh38.p14 chr 20	NC_000020.11:g.38919003CA[12]
GRCh37.p13 chr 20	NC_000020.10:g.37547646CA[7]
GRCh37.p13 chr 20	NC_000020.10:g.37547646CA[8]
GRCh37.p13 chr 20	NC_000020.10:g.37547646CA[10]
GRCh37.p13 chr 20	NC_000020.10:g.37547646CA[11]
GRCh37.p13 chr 20	NC_000020.10:g.37547646CA[12]

Gene: PPP1R16B, protein phosphatase 1 regulatory subunit 16B (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PPP1R16B transcript variant 1	NM_015568.4:c.336_354=	N/A	3 Prime UTR Variant
PPP1R16B transcript variant 2	NM_001172735.3:c.336_35… NM_001172735.3:c.336_354=	N/A	3 Prime UTR Variant
PPP1R16B transcript variant X1	XM_011528768.4:c.336_35… XM_011528768.4:c.336_354=	N/A	3 Prime UTR Variant
PPP1R16B transcript variant X2	XM_047440086.1:c.336_35… XM_047440086.1:c.336_354=	N/A	3 Prime UTR 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	(AC)₉A=	delCACA	delCA	dupCA	dupCACA	dup(CA)₃
GRCh38.p14 chr 20	NC_000020.11:g.38919002_38919020=	NC_000020.11:g.38919003CA[7]	NC_000020.11:g.38919003CA[8]	NC_000020.11:g.38919003CA[10]	NC_000020.11:g.38919003CA[11]	NC_000020.11:g.38919003CA[12]
GRCh37.p13 chr 20	NC_000020.10:g.37547645_37547663=	NC_000020.10:g.37547646CA[7]	NC_000020.10:g.37547646CA[8]	NC_000020.10:g.37547646CA[10]	NC_000020.10:g.37547646CA[11]	NC_000020.10:g.37547646CA[12]
PPP1R16B transcript variant X1	XM_011528768.4:c.336_354=	XM_011528768.4:c.*337CA[7]	XM_011528768.4:c.*337CA[8]	XM_011528768.4:c.*337CA[10]	XM_011528768.4:c.*337CA[11]	XM_011528768.4:c.*337CA[12]
PPP1R16B transcript variant X1	XM_011528768.3:c.336_354=	XM_011528768.3:c.*337CA[7]	XM_011528768.3:c.*337CA[8]	XM_011528768.3:c.*337CA[10]	XM_011528768.3:c.*337CA[11]	XM_011528768.3:c.*337CA[12]
PPP1R16B transcript variant X1	XM_011528768.2:c.336_354=	XM_011528768.2:c.*337CA[7]	XM_011528768.2:c.*337CA[8]	XM_011528768.2:c.*337CA[10]	XM_011528768.2:c.*337CA[11]	XM_011528768.2:c.*337CA[12]
PPP1R16B transcript variant X1	XM_011528768.1:c.336_354=	XM_011528768.1:c.*337CA[7]	XM_011528768.1:c.*337CA[8]	XM_011528768.1:c.*337CA[10]	XM_011528768.1:c.*337CA[11]	XM_011528768.1:c.*337CA[12]
PPP1R16B transcript variant 1	NM_015568.4:c.336_354=	NM_015568.4:c.*337CA[7]	NM_015568.4:c.*337CA[8]	NM_015568.4:c.*337CA[10]	NM_015568.4:c.*337CA[11]	NM_015568.4:c.*337CA[12]
PPP1R16B transcript variant 1	NM_015568.3:c.336_354=	NM_015568.3:c.*337CA[7]	NM_015568.3:c.*337CA[8]	NM_015568.3:c.*337CA[10]	NM_015568.3:c.*337CA[11]	NM_015568.3:c.*337CA[12]
PPP1R16B transcript variant 1	NM_015568.2:c.336_354=	NM_015568.2:c.*337CA[7]	NM_015568.2:c.*337CA[8]	NM_015568.2:c.*337CA[10]	NM_015568.2:c.*337CA[11]	NM_015568.2:c.*337CA[12]
PPP1R16B transcript variant 2	NM_001172735.3:c.336_354=	NM_001172735.3:c.*337CA[7]	NM_001172735.3:c.*337CA[8]	NM_001172735.3:c.*337CA[10]	NM_001172735.3:c.*337CA[11]	NM_001172735.3:c.*337CA[12]
PPP1R16B transcript variant 2	NM_001172735.2:c.336_354=	NM_001172735.2:c.*337CA[7]	NM_001172735.2:c.*337CA[8]	NM_001172735.2:c.*337CA[10]	NM_001172735.2:c.*337CA[11]	NM_001172735.2:c.*337CA[12]
PPP1R16B transcript variant 2	NM_001172735.1:c.336_354=	NM_001172735.1:c.*337CA[7]	NM_001172735.1:c.*337CA[8]	NM_001172735.1:c.*337CA[10]	NM_001172735.1:c.*337CA[11]	NM_001172735.1:c.*337CA[12]
PPP1R16B transcript variant X2	XM_047440086.1:c.336_354=	XM_047440086.1:c.*337CA[7]	XM_047440086.1:c.*337CA[8]	XM_047440086.1:c.*337CA[10]	XM_047440086.1:c.*337CA[11]	XM_047440086.1:c.*337CA[12]

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#.

54 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41406224	Oct 12, 2018 (152)
2	HGSV	ss81083381	Oct 12, 2018 (152)
3	GMI	ss289410976	May 04, 2012 (137)
4	1000GENOMES	ss327945299	May 09, 2011 (134)
5	1000GENOMES	ss328062010	May 09, 2011 (134)
6	1000GENOMES	ss328296503	May 09, 2011 (134)
7	LUNTER	ss552661825	Apr 25, 2013 (138)
8	LUNTER	ss553064639	Apr 25, 2013 (138)
9	LUNTER	ss553679152	Apr 25, 2013 (138)
10	TISHKOFF	ss566009602	Apr 25, 2013 (138)
11	SSMP	ss664474220	Apr 01, 2015 (144)
12	1000GENOMES	ss1378486552	Aug 21, 2014 (142)
13	DDI	ss1536908205	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1709356792	Jan 10, 2018 (151)
15	EVA_UK10K_TWINSUK	ss1709357213	Jan 10, 2018 (151)
16	EVA_UK10K_TWINSUK	ss1710813341	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1710813342	Apr 01, 2015 (144)
18	HAMMER_LAB	ss1809498503	Sep 08, 2015 (146)
19	SYSTEMSBIOZJU	ss2629440213	Nov 08, 2017 (151)
20	SWEGEN	ss3018175863	Nov 08, 2017 (151)
21	SWEGEN	ss3018175864	Nov 08, 2017 (151)
22	MCHAISSO	ss3063998114	Nov 08, 2017 (151)
23	EVA_DECODE	ss3706935434	Jul 13, 2019 (153)
24	EVA_DECODE	ss3706935435	Jul 13, 2019 (153)
25	EVA_DECODE	ss3706935436	Jul 13, 2019 (153)
26	EVA_DECODE	ss3706935437	Jul 13, 2019 (153)
27	ACPOP	ss3743388273	Jul 13, 2019 (153)
28	ACPOP	ss3743388274	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3821798984	Jul 13, 2019 (153)
30	EVA	ss3835669206	Apr 27, 2020 (154)
31	KOGIC	ss3982272434	Apr 27, 2020 (154)
32	KOGIC	ss3982272435	Apr 27, 2020 (154)
33	GNOMAD	ss4353325687	Apr 27, 2021 (155)
34	GNOMAD	ss4353325688	Apr 27, 2021 (155)
35	GNOMAD	ss4353325689	Apr 27, 2021 (155)
36	GNOMAD	ss4353325690	Apr 27, 2021 (155)
37	GNOMAD	ss4353325691	Apr 27, 2021 (155)
38	TOPMED	ss5088430533	Apr 27, 2021 (155)
39	TOMMO_GENOMICS	ss5229628476	Apr 27, 2021 (155)
40	TOMMO_GENOMICS	ss5229628477	Apr 27, 2021 (155)
41	TOMMO_GENOMICS	ss5229628478	Apr 27, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5308782018	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5308782019	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5501060700	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5501060701	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5501060702	Oct 16, 2022 (156)
47	EVA	ss5512214662	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5789425415	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5789425416	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5789425417	Oct 16, 2022 (156)
51	YY_MCH	ss5818040891	Oct 16, 2022 (156)
52	EVA	ss5845686523	Oct 16, 2022 (156)
53	EVA	ss5845686524	Oct 16, 2022 (156)
54	EVA	ss5853137938	Oct 16, 2022 (156)
55	1000Genomes	NC_000020.10 - 37547645	Oct 12, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 43292970 (NC_000020.10:37547644::AC 678/3854) Row 43292971 (NC_000020.10:37547644:AC: 72/3854)	-	Oct 12, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 43292970 (NC_000020.10:37547644::AC 678/3854) Row 43292971 (NC_000020.10:37547644:AC: 72/3854)	-	Oct 12, 2018 (152)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551723973 (NC_000020.11:38919001::AC 27661/138672) Row 551723974 (NC_000020.11:38919001::ACAC 210/138732) Row 551723975 (NC_000020.11:38919001::ACACAC 29/138732)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551723973 (NC_000020.11:38919001::AC 27661/138672) Row 551723974 (NC_000020.11:38919001::ACAC 210/138732) Row 551723975 (NC_000020.11:38919001::ACACAC 29/138732)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551723973 (NC_000020.11:38919001::AC 27661/138672) Row 551723974 (NC_000020.11:38919001::ACAC 210/138732) Row 551723975 (NC_000020.11:38919001::ACACAC 29/138732)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551723973 (NC_000020.11:38919001::AC 27661/138672) Row 551723974 (NC_000020.11:38919001::ACAC 210/138732) Row 551723975 (NC_000020.11:38919001::ACACAC 29/138732)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551723973 (NC_000020.11:38919001::AC 27661/138672) Row 551723974 (NC_000020.11:38919001::ACAC 210/138732) Row 551723975 (NC_000020.11:38919001::ACACAC 29/138732)...	-	Apr 27, 2021 (155)
63	Korean Genome Project Submission ignored due to conflicting rows: Row 38650435 (NC_000020.11:38919003::AC 443/1832) Row 38650436 (NC_000020.11:38919001:AC: 12/1832)	-	Apr 27, 2020 (154)
64	Korean Genome Project Submission ignored due to conflicting rows: Row 38650435 (NC_000020.11:38919003::AC 443/1832) Row 38650436 (NC_000020.11:38919001:AC: 12/1832)	-	Apr 27, 2020 (154)
65	Northern Sweden Submission ignored due to conflicting rows: Row 16673138 (NC_000020.10:37547644::AC 105/600) Row 16673139 (NC_000020.10:37547644::ACAC 1/600)	-	Jul 13, 2019 (153)
66	Northern Sweden Submission ignored due to conflicting rows: Row 16673138 (NC_000020.10:37547644::AC 105/600) Row 16673139 (NC_000020.10:37547644::ACAC 1/600)	-	Jul 13, 2019 (153)
67	8.3KJPN Submission ignored due to conflicting rows: Row 87597783 (NC_000020.10:37547644::AC 4073/16760) Row 87597784 (NC_000020.10:37547644::ACAC 21/16760) Row 87597785 (NC_000020.10:37547644:AC: 6/16760)	-	Apr 27, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 87597783 (NC_000020.10:37547644::AC 4073/16760) Row 87597784 (NC_000020.10:37547644::ACAC 21/16760) Row 87597785 (NC_000020.10:37547644:AC: 6/16760)	-	Apr 27, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 87597783 (NC_000020.10:37547644::AC 4073/16760) Row 87597784 (NC_000020.10:37547644::ACAC 21/16760) Row 87597785 (NC_000020.10:37547644:AC: 6/16760)	-	Apr 27, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 123262519 (NC_000020.11:38919001::AC 6928/28258) Row 123262520 (NC_000020.11:38919001::ACAC 35/28258) Row 123262521 (NC_000020.11:38919001:AC: 6/28258)	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 123262519 (NC_000020.11:38919001::AC 6928/28258) Row 123262520 (NC_000020.11:38919001::ACAC 35/28258) Row 123262521 (NC_000020.11:38919001:AC: 6/28258)	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 123262519 (NC_000020.11:38919001::AC 6928/28258) Row 123262520 (NC_000020.11:38919001::ACAC 35/28258) Row 123262521 (NC_000020.11:38919001:AC: 6/28258)	-	Oct 16, 2022 (156)
73	TopMed	NC_000020.11 - 38919002	Apr 27, 2021 (155)
74	UK 10K study - Twins Submission ignored due to conflicting rows: Row 43292970 (NC_000020.10:37547644::AC 687/3708) Row 43292971 (NC_000020.10:37547644:AC: 68/3708)	-	Oct 12, 2018 (152)
75	UK 10K study - Twins Submission ignored due to conflicting rows: Row 43292970 (NC_000020.10:37547644::AC 687/3708) Row 43292971 (NC_000020.10:37547644:AC: 68/3708)	-	Oct 12, 2018 (152)
76	ALFA	NC_000020.11 - 38919002	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)
rs60130384	May 25, 2008 (130)
rs72385269	May 15, 2013 (138)
rs797010755	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4353325691	NC_000020.11:38919001:ACAC:	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACA	(self)
ss3706935437	NC_000020.11:38919016:CACA:	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACA	(self)
ss1709356792, ss1709357213, ss5229628478, ss5512214662, ss5845686524	NC_000020.10:37547644:AC:	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACA	(self)
ss3982272435, ss4353325690, ss5501060700, ss5789425417	NC_000020.11:38919001:AC:	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACA	(self)
1620887885	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACA	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACA	(self)
ss3706935436	NC_000020.11:38919018:CA:	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACA	(self)
ss327945299, ss328062010, ss328296503, ss552661825, ss553064639, ss553679152	NC_000020.9:36981058::AC	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss289410976	NC_000020.9:36981077::CA	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACA	(self)
78211995, ss664474220, ss1378486552, ss1536908205, ss1809498503, ss2629440213, ss3018175863, ss3743388273, ss3835669206, ss5229628476, ss5845686523	NC_000020.10:37547644::AC	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss1710813341, ss1710813342	NC_000020.10:37547646::AC	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss566009602	NC_000020.10:37547663::CA	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss3063998114, ss3821798984, ss4353325687, ss5308782018, ss5501060701, ss5789425415, ss5818040891, ss5853137938	NC_000020.11:38919001::AC	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACA	(self)
1620887885	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACA	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss3982272434	NC_000020.11:38919003::AC	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss3706935435	NC_000020.11:38919020::CA	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss41406224, ss81083381	NT_011362.10:7743755::CA	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACA	(self)
ss3018175864, ss3743388274, ss5229628477	NC_000020.10:37547644::ACAC	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss4353325688, ss5308782019, ss5789425416	NC_000020.11:38919001::ACAC	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACACA	(self)
1620887885	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACACA	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3706935434	NC_000020.11:38919020::CACA	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACACA	(self)
363539478, ss4353325689, ss5088430533, ss5501060702	NC_000020.11:38919001::ACACAC	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
1620887885	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACACACA	NC_000020.11:38919001:ACACACACACAC… NC_000020.11:38919001:ACACACACACACACACACA:ACACACACACACACACACACACACA	(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 rs35869936

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs35869936