Name: rs111469369
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.

rs111469369

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:13876693-13876707 (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(CA)₃ / delCACA / delCA / dupCA…
del(CA)₃ / delCACA / delCA / dupCA / dupCACA / dup(CA)₃ / dup(CA)₄
Variation Type: Indel Insertion and Deletion
Frequency: dupCA=0.08471 (882/10412, ALFA)
dupCA=0.3492 (1749/5008, 1000G)
dupCA=0.1988 (887/4462, Estonian) (+ 1 more)
dupCA=0.316 (67/212, Vietnamese)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NANOS3 : 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	10412	ACACACACACACACA=0.91452	ACACACACACACA=0.00000, ACACACACACACACACA=0.08471, ACACACACACACACACACA=0.00077, ACACACACACACACACACACA=0.00000, ACACACACACACACACACACACA=0.00000	0.847249	0.016737	0.136014	32
European	Sub	9200	ACACACACACACACA=0.9034	ACACACACACACA=0.0000, ACACACACACACACACA=0.0958, ACACACACACACACACACA=0.0009, ACACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000	0.827308	0.018946	0.153746	31
African	Sub	468	ACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	18	ACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
African American	Sub	450	ACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	54	ACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	46	ACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	ACACACACACACACA=1.0	ACACACACACACA=0.0, ACACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACA=0.0, ACACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	82	ACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	336	ACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	52	ACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other	Sub	220	ACACACACACACACA=0.995	ACACACACACACA=0.000, ACACACACACACACACA=0.005, ACACACACACACACACACA=0.000, ACACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000	0.990909	0.0	0.009091	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	10412	(AC)₇A=0.91452	delCA=0.00000, dupCA=0.08471, dupCACA=0.00077, dup(CA)₃=0.00000, dup(CA)₄=0.00000
Allele Frequency Aggregator	European	Sub	9200	(AC)₇A=0.9034	delCA=0.0000, dupCA=0.0958, dupCACA=0.0009, dup(CA)₃=0.0000, dup(CA)₄=0.0000
Allele Frequency Aggregator	African	Sub	468	(AC)₇A=1.000	delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	336	(AC)₇A=1.000	delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000
Allele Frequency Aggregator	Other	Sub	220	(AC)₇A=0.995	delCA=0.000, dupCA=0.005, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	82	(AC)₇A=1.00	delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00
Allele Frequency Aggregator	Asian	Sub	54	(AC)₇A=1.00	delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	52	(AC)₇A=1.00	delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupCA=0.3492
1000Genomes	African	Sub	1322	- No frequency provided	dupCA=0.5772
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupCA=0.3135
1000Genomes	Europe	Sub	1006	- No frequency provided	dupCA=0.2078
1000Genomes	South Asian	Sub	978	- No frequency provided	dupCA=0.310
1000Genomes	American	Sub	694	- No frequency provided	dupCA=0.228
Genetic variation in the Estonian population	Estonian	Study-wide	4462	- No frequency provided	dupCA=0.1988
A Vietnamese Genetic Variation Database	Global	Study-wide	212	- No frequency provided	dupCA=0.316

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 19	NC_000019.10:g.13876694CA[4]
GRCh38.p14 chr 19	NC_000019.10:g.13876694CA[5]
GRCh38.p14 chr 19	NC_000019.10:g.13876694CA[6]
GRCh38.p14 chr 19	NC_000019.10:g.13876694CA[8]
GRCh38.p14 chr 19	NC_000019.10:g.13876694CA[9]
GRCh38.p14 chr 19	NC_000019.10:g.13876694CA[10]
GRCh38.p14 chr 19	NC_000019.10:g.13876694CA[11]
GRCh37.p13 chr 19	NC_000019.9:g.13987508CA[4]
GRCh37.p13 chr 19	NC_000019.9:g.13987508CA[5]
GRCh37.p13 chr 19	NC_000019.9:g.13987508CA[6]
GRCh37.p13 chr 19	NC_000019.9:g.13987508CA[8]
GRCh37.p13 chr 19	NC_000019.9:g.13987508CA[9]
GRCh37.p13 chr 19	NC_000019.9:g.13987508CA[10]
GRCh37.p13 chr 19	NC_000019.9:g.13987508CA[11]
GRCh38.p14 chr 19 fix patch HG109_PATCH	NW_021160022.1:g.88535CA[4]
GRCh38.p14 chr 19 fix patch HG109_PATCH	NW_021160022.1:g.88535CA[5]
GRCh38.p14 chr 19 fix patch HG109_PATCH	NW_021160022.1:g.88535CA[6]
GRCh38.p14 chr 19 fix patch HG109_PATCH	NW_021160022.1:g.88535CA[8]
GRCh38.p14 chr 19 fix patch HG109_PATCH	NW_021160022.1:g.88535CA[9]
GRCh38.p14 chr 19 fix patch HG109_PATCH	NW_021160022.1:g.88535CA[10]
GRCh38.p14 chr 19 fix patch HG109_PATCH	NW_021160022.1:g.88535CA[11]

Gene: NANOS3, nanos C2HC-type zinc finger 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NANOS3 transcript variant 1	NM_001098622.3:c.	N/A	Genic Upstream Transcript Variant
NANOS3 transcript variant 2	NR_146095.2:n.	N/A	Intron Variant
NANOS3 transcript variant 3	NR_146096.2:n.	N/A	Intron Variant
NANOS3 transcript variant 4	NR_146097.2: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	(AC)₇A=	del(CA)₃	delCACA	delCA	dupCA	dupCACA	dup(CA)₃	dup(CA)₄
GRCh38.p14 chr 19	NC_000019.10:g.13876693_13876707=	NC_000019.10:g.13876694CA[4]	NC_000019.10:g.13876694CA[5]	NC_000019.10:g.13876694CA[6]	NC_000019.10:g.13876694CA[8]	NC_000019.10:g.13876694CA[9]	NC_000019.10:g.13876694CA[10]	NC_000019.10:g.13876694CA[11]
GRCh37.p13 chr 19	NC_000019.9:g.13987507_13987521=	NC_000019.9:g.13987508CA[4]	NC_000019.9:g.13987508CA[5]	NC_000019.9:g.13987508CA[6]	NC_000019.9:g.13987508CA[8]	NC_000019.9:g.13987508CA[9]	NC_000019.9:g.13987508CA[10]	NC_000019.9:g.13987508CA[11]
GRCh38.p14 chr 19 fix patch HG109_PATCH	NW_021160022.1:g.88534_88548=	NW_021160022.1:g.88535CA[4]	NW_021160022.1:g.88535CA[5]	NW_021160022.1:g.88535CA[6]	NW_021160022.1:g.88535CA[8]	NW_021160022.1:g.88535CA[9]	NW_021160022.1:g.88535CA[10]	NW_021160022.1:g.88535CA[11]

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#.

60 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81732169	Dec 03, 2013 (138)
2	HGSV	ss82013403	Dec 04, 2013 (138)
3	HGSV	ss82530704	Dec 04, 2013 (138)
4	BUSHMAN	ss193499696	Jul 04, 2010 (132)
5	GMI	ss289377394	May 04, 2012 (137)
6	GMI	ss289377395	Oct 12, 2018 (152)
7	1000GENOMES	ss327885745	May 09, 2011 (135)
8	1000GENOMES	ss328018672	May 09, 2011 (135)
9	1000GENOMES	ss328267947	May 09, 2011 (135)
10	LUNTER	ss552607162	Apr 25, 2013 (138)
11	LUNTER	ss552989532	Apr 25, 2013 (138)
12	LUNTER	ss553656304	Apr 25, 2013 (138)
13	SSMP	ss664426556	Apr 01, 2015 (144)
14	1000GENOMES	ss1377987021	Aug 21, 2014 (142)
15	DDI	ss1536885533	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1709131635	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1709131636	Apr 01, 2015 (144)
18	EVA_UK10K_TWINSUK	ss1709131641	Apr 01, 2015 (144)
19	EVA_UK10K_TWINSUK	ss1709131643	Apr 01, 2015 (144)
20	HAMMER_LAB	ss1809219926	Sep 08, 2015 (146)
21	SWEGEN	ss3017144405	Nov 08, 2017 (151)
22	SWEGEN	ss3017144406	Nov 08, 2017 (151)
23	MCHAISSO	ss3063908690	Nov 08, 2017 (151)
24	MCHAISSO	ss3065702371	Nov 08, 2017 (151)
25	URBANLAB	ss3650872712	Oct 12, 2018 (152)
26	EGCUT_WGS	ss3683970865	Jul 13, 2019 (153)
27	EVA_DECODE	ss3702397687	Jul 13, 2019 (153)
28	EVA_DECODE	ss3702397688	Jul 13, 2019 (153)
29	EVA_DECODE	ss3702397689	Jul 13, 2019 (153)
30	EVA_DECODE	ss3702397690	Jul 13, 2019 (153)
31	ACPOP	ss3742876965	Jul 13, 2019 (153)
32	ACPOP	ss3742876966	Jul 13, 2019 (153)
33	KHV_HUMAN_GENOMES	ss3821096062	Jul 13, 2019 (153)
34	EVA	ss3835364807	Apr 27, 2020 (154)
35	EVA	ss3841302654	Apr 27, 2020 (154)
36	EVA	ss3846807238	Apr 27, 2020 (154)
37	KOGIC	ss3980902045	Apr 27, 2020 (154)
38	KOGIC	ss3980902046	Apr 27, 2020 (154)
39	GNOMAD	ss4328110015	Apr 26, 2021 (155)
40	GNOMAD	ss4328110016	Apr 26, 2021 (155)
41	GNOMAD	ss4328110017	Apr 26, 2021 (155)
42	GNOMAD	ss4328110018	Apr 26, 2021 (155)
43	GNOMAD	ss4328110019	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5226875878	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5226875879	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5226875880	Apr 26, 2021 (155)
47	1000G_HIGH_COVERAGE	ss5306591940	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5306591941	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5499207197	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5499207198	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5499207199	Oct 16, 2022 (156)
52	SANFORD_IMAGENETICS	ss5662028607	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5785203006	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5785203007	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5785203008	Oct 16, 2022 (156)
56	YY_MCH	ss5817430497	Oct 16, 2022 (156)
57	EVA	ss5840291639	Oct 16, 2022 (156)
58	EVA	ss5840291640	Oct 16, 2022 (156)
59	EVA	ss5840291641	Oct 16, 2022 (156)
60	EVA	ss5852214379	Oct 16, 2022 (156)
61	1000Genomes	NC_000019.9 - 13987507	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 42014277 (NC_000019.9:13987506::AC 781/3854) Row 42014278 (NC_000019.9:13987506::ACAC 40/3854)	-	Oct 12, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 42014277 (NC_000019.9:13987506::AC 781/3854) Row 42014278 (NC_000019.9:13987506::ACAC 40/3854)	-	Oct 12, 2018 (152)
64	Genetic variation in the Estonian population	NC_000019.9 - 13987507	Oct 12, 2018 (152)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534832572 (NC_000019.10:13876692::AC 43583/139546) Row 534832573 (NC_000019.10:13876692::ACAC 630/139612) Row 534832574 (NC_000019.10:13876692::ACACAC 2/139614)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534832572 (NC_000019.10:13876692::AC 43583/139546) Row 534832573 (NC_000019.10:13876692::ACAC 630/139612) Row 534832574 (NC_000019.10:13876692::ACACAC 2/139614)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534832572 (NC_000019.10:13876692::AC 43583/139546) Row 534832573 (NC_000019.10:13876692::ACAC 630/139612) Row 534832574 (NC_000019.10:13876692::ACACAC 2/139614)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534832572 (NC_000019.10:13876692::AC 43583/139546) Row 534832573 (NC_000019.10:13876692::ACAC 630/139612) Row 534832574 (NC_000019.10:13876692::ACACAC 2/139614)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534832572 (NC_000019.10:13876692::AC 43583/139546) Row 534832573 (NC_000019.10:13876692::ACAC 630/139612) Row 534832574 (NC_000019.10:13876692::ACACAC 2/139614)...	-	Apr 26, 2021 (155)
70	Korean Genome Project Submission ignored due to conflicting rows: Row 37280046 (NC_000019.10:13876694::AC 528/1832) Row 37280047 (NC_000019.10:13876692:AC: 5/1832)	-	Apr 27, 2020 (154)
71	Korean Genome Project Submission ignored due to conflicting rows: Row 37280046 (NC_000019.10:13876694::AC 528/1832) Row 37280047 (NC_000019.10:13876692:AC: 5/1832)	-	Apr 27, 2020 (154)
72	Northern Sweden Submission ignored due to conflicting rows: Row 16161830 (NC_000019.9:13987506::AC 135/600) Row 16161831 (NC_000019.9:13987506::ACAC 10/600)	-	Jul 13, 2019 (153)
73	Northern Sweden Submission ignored due to conflicting rows: Row 16161830 (NC_000019.9:13987506::AC 135/600) Row 16161831 (NC_000019.9:13987506::ACAC 10/600)	-	Jul 13, 2019 (153)
74	8.3KJPN Submission ignored due to conflicting rows: Row 84845185 (NC_000019.9:13987506::AC 4841/16758) Row 84845186 (NC_000019.9:13987506:ACACAC: 2/16758) Row 84845187 (NC_000019.9:13987506::ACACAC 1/16758)	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 84845185 (NC_000019.9:13987506::AC 4841/16758) Row 84845186 (NC_000019.9:13987506:ACACAC: 2/16758) Row 84845187 (NC_000019.9:13987506::ACACAC 1/16758)	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 84845185 (NC_000019.9:13987506::AC 4841/16758) Row 84845186 (NC_000019.9:13987506:ACACAC: 2/16758) Row 84845187 (NC_000019.9:13987506::ACACAC 1/16758)	-	Apr 26, 2021 (155)
77	14KJPN Submission ignored due to conflicting rows: Row 119040110 (NC_000019.10:13876692::AC 8192/28258) Row 119040111 (NC_000019.10:13876692:ACACAC: 3/28258) Row 119040112 (NC_000019.10:13876692::ACACAC 2/28258)	-	Oct 16, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 119040110 (NC_000019.10:13876692::AC 8192/28258) Row 119040111 (NC_000019.10:13876692:ACACAC: 3/28258) Row 119040112 (NC_000019.10:13876692::ACACAC 2/28258)	-	Oct 16, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 119040110 (NC_000019.10:13876692::AC 8192/28258) Row 119040111 (NC_000019.10:13876692:ACACAC: 3/28258) Row 119040112 (NC_000019.10:13876692::ACACAC 2/28258)	-	Oct 16, 2022 (156)
80	UK 10K study - Twins Submission ignored due to conflicting rows: Row 42014277 (NC_000019.9:13987506::AC 772/3708) Row 42014278 (NC_000019.9:13987506::ACAC 32/3708)	-	Oct 12, 2018 (152)
81	UK 10K study - Twins Submission ignored due to conflicting rows: Row 42014277 (NC_000019.9:13987506::AC 772/3708) Row 42014278 (NC_000019.9:13987506::ACAC 32/3708)	-	Oct 12, 2018 (152)
82	A Vietnamese Genetic Variation Database	NC_000019.9 - 13987507	Jul 13, 2019 (153)
83	ALFA	NC_000019.10 - 13876693	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)
rs138471152	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5226875879	NC_000019.9:13987506:ACACAC:	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACA	(self)
ss5785203007	NC_000019.10:13876692:ACACAC:	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACA
ss3702397690	NC_000019.10:13876692:ACAC:	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACA	(self)
ss5840291640	NC_000019.9:13987506:AC:	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACA
ss3980902046, ss4328110019, ss5499207198	NC_000019.10:13876692:AC:	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACA	(self)
12726315664	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACA	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACA	(self)
ss3702397689	NC_000019.10:13876694:AC:	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACA	(self)
ss289377394, ss327885745, ss328018672, ss328267947, ss552607162, ss552989532, ss553656304	NC_000019.8:13848506::AC	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACA	(self)
ss289377395	NC_000019.8:13848521::CA	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACA	(self)
75834007, 29709113, 9285831, ss664426556, ss1377987021, ss1536885533, ss1709131635, ss1709131641, ss1809219926, ss3017144405, ss3683970865, ss3742876965, ss3835364807, ss3841302654, ss5226875878, ss5662028607, ss5840291639	NC_000019.9:13987506::AC	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACA	(self)
ss3063908690, ss3065702371, ss3650872712, ss3821096062, ss3846807238, ss4328110015, ss5306591940, ss5499207197, ss5785203006, ss5817430497, ss5852214379	NC_000019.10:13876692::AC	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACA	(self)
12726315664	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACA	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACA	(self)
ss3980902045	NC_000019.10:13876694::AC	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACA	(self)
ss3702397688	NC_000019.10:13876696::AC	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACA	(self)
ss81732169, ss82013403, ss82530704	NT_011295.11:5250323::CA	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACA	(self)
ss193499696	NT_011295.12:13816692::AC	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACA	(self)
ss1709131636, ss1709131643, ss3017144406, ss3742876966, ss5840291641	NC_000019.9:13987506::ACAC	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACACA	(self)
ss4328110016, ss5306591941, ss5499207199	NC_000019.10:13876692::ACAC	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACACA	(self)
12726315664	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACACA	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACACA	(self)
ss3702397687	NC_000019.10:13876696::ACAC	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACACA	(self)
ss5226875880	NC_000019.9:13987506::ACACAC	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACACACA	(self)
ss4328110017, ss5785203008	NC_000019.10:13876692::ACACAC	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACACACA	(self)
12726315664	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACACACA	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACACACA	(self)
ss4328110018	NC_000019.10:13876692::ACACACAC	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACACACACA	(self)
12726315664	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACACACACA	NC_000019.10:13876692:ACACACACACAC… NC_000019.10:13876692:ACACACACACACACA:ACACACACACACACACACACACA	(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 rs111469369

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

rs111469369