Name: rs11420509
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.

rs11420509

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:112100712-112100730 (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(T)₆ / del(T)₄ / delTTT / delTT…
del(T)₆ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₁₀ / ins(T)₁₀G(T)₂₁ / ins(T)₃₇
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1153 (824/7144, ALFA)
delT=0.0387 (194/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SOX1-OT : 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	7144	TTTTTTTTTTTTTTTTTTT=0.7814	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.1153, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0941, TTTTTTTTTTTTTTTTTTTTTTTT=0.0035, TTTTTTTTTTTTTTTTTTTTTTT=0.0039, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0018	0.832095	0.063514	0.104392	32
European	Sub	6374	TTTTTTTTTTTTTTTTTTT=0.7553	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.1293, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.1051, TTTTTTTTTTTTTTTTTTTTTTTT=0.0039, TTTTTTTTTTTTTTTTTTTTTTT=0.0044, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0020	0.80714	0.072953	0.119907	32
African	Sub	406	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	10	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	396	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	28	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	26	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	42	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	168	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	10	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	116	TTTTTTTTTTTTTTTTTTT=0.983	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.017, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	7144	(T)₁₉=0.7814	del(T)₆=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1153, dupTT=0.0000, dupTTT=0.0941, dup(T)₄=0.0039, dup(T)₅=0.0035, dup(T)₆=0.0018
Allele Frequency Aggregator	European	Sub	6374	(T)₁₉=0.7553	del(T)₆=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1293, dupTT=0.0000, dupTTT=0.1051, dup(T)₄=0.0044, dup(T)₅=0.0039, dup(T)₆=0.0020
Allele Frequency Aggregator	African	Sub	406	(T)₁₉=1.000	del(T)₆=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	168	(T)₁₉=1.000	del(T)₆=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Other	Sub	116	(T)₁₉=0.983	del(T)₆=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.017, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	42	(T)₁₉=1.00	del(T)₆=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Asian	Sub	28	(T)₁₉=1.00	del(T)₆=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	10	(T)₁₉=1.0	del(T)₆=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0
1000Genomes	Global	Study-wide	5008	(T)₁₉=0.9613	delT=0.0387
1000Genomes	African	Sub	1322	(T)₁₉=0.9682	delT=0.0318
1000Genomes	East Asian	Sub	1008	(T)₁₉=0.9524	delT=0.0476
1000Genomes	Europe	Sub	1006	(T)₁₉=0.9563	delT=0.0437
1000Genomes	South Asian	Sub	978	(T)₁₉=0.976	delT=0.024
1000Genomes	American	Sub	694	(T)₁₉=0.947	delT=0.053

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 13	NC_000013.11:g.112100725_112100730del
GRCh38.p14 chr 13	NC_000013.11:g.112100727_112100730del
GRCh38.p14 chr 13	NC_000013.11:g.112100728_112100730del
GRCh38.p14 chr 13	NC_000013.11:g.112100729_112100730del
GRCh38.p14 chr 13	NC_000013.11:g.112100730del
GRCh38.p14 chr 13	NC_000013.11:g.112100730dup
GRCh38.p14 chr 13	NC_000013.11:g.112100729_112100730dup
GRCh38.p14 chr 13	NC_000013.11:g.112100728_112100730dup
GRCh38.p14 chr 13	NC_000013.11:g.112100727_112100730dup
GRCh38.p14 chr 13	NC_000013.11:g.112100726_112100730dup
GRCh38.p14 chr 13	NC_000013.11:g.112100725_112100730dup
GRCh38.p14 chr 13	NC_000013.11:g.112100724_112100730dup
GRCh38.p14 chr 13	NC_000013.11:g.112100723_112100730dup
GRCh38.p14 chr 13	NC_000013.11:g.112100721_112100730dup
GRCh38.p14 chr 13	NC_000013.11:g.112100712_112100730T[29]GTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 13	NC_000013.11:g.112100730_112100731insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 13	NC_000013.10:g.112755039_112755044del
GRCh37.p13 chr 13	NC_000013.10:g.112755041_112755044del
GRCh37.p13 chr 13	NC_000013.10:g.112755042_112755044del
GRCh37.p13 chr 13	NC_000013.10:g.112755043_112755044del
GRCh37.p13 chr 13	NC_000013.10:g.112755044del
GRCh37.p13 chr 13	NC_000013.10:g.112755044dup
GRCh37.p13 chr 13	NC_000013.10:g.112755043_112755044dup
GRCh37.p13 chr 13	NC_000013.10:g.112755042_112755044dup
GRCh37.p13 chr 13	NC_000013.10:g.112755041_112755044dup
GRCh37.p13 chr 13	NC_000013.10:g.112755040_112755044dup
GRCh37.p13 chr 13	NC_000013.10:g.112755039_112755044dup
GRCh37.p13 chr 13	NC_000013.10:g.112755038_112755044dup
GRCh37.p13 chr 13	NC_000013.10:g.112755037_112755044dup
GRCh37.p13 chr 13	NC_000013.10:g.112755035_112755044dup
GRCh37.p13 chr 13	NC_000013.10:g.112755026_112755044T[29]GTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 13	NC_000013.10:g.112755044_112755045insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: SOX1-OT, SOX1 overlapping transcript (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SOX1-OT transcript variant 1	NR_120392.1:n.	N/A	Intron Variant
SOX1-OT transcript variant 2	NR_120394.1:n.	N/A	Genic Upstream Transcript 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	(T)₁₉=	del(T)₆	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₁₀	ins(T)₁₀G(T)₂₁	ins(T)₃₇
GRCh38.p14 chr 13	NC_000013.11:g.112100712_112100730=	NC_000013.11:g.112100725_112100730del	NC_000013.11:g.112100727_112100730del	NC_000013.11:g.112100728_112100730del	NC_000013.11:g.112100729_112100730del	NC_000013.11:g.112100730del	NC_000013.11:g.112100730dup	NC_000013.11:g.112100729_112100730dup	NC_000013.11:g.112100728_112100730dup	NC_000013.11:g.112100727_112100730dup	NC_000013.11:g.112100726_112100730dup	NC_000013.11:g.112100725_112100730dup	NC_000013.11:g.112100724_112100730dup	NC_000013.11:g.112100723_112100730dup	NC_000013.11:g.112100721_112100730dup	NC_000013.11:g.112100712_112100730T[29]GTTTTTTTTTTTTTTTTTTTTT[1]	NC_000013.11:g.112100730_112100731insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 13	NC_000013.10:g.112755026_112755044=	NC_000013.10:g.112755039_112755044del	NC_000013.10:g.112755041_112755044del	NC_000013.10:g.112755042_112755044del	NC_000013.10:g.112755043_112755044del	NC_000013.10:g.112755044del	NC_000013.10:g.112755044dup	NC_000013.10:g.112755043_112755044dup	NC_000013.10:g.112755042_112755044dup	NC_000013.10:g.112755041_112755044dup	NC_000013.10:g.112755040_112755044dup	NC_000013.10:g.112755039_112755044dup	NC_000013.10:g.112755038_112755044dup	NC_000013.10:g.112755037_112755044dup	NC_000013.10:g.112755035_112755044dup	NC_000013.10:g.112755026_112755044T[29]GTTTTTTTTTTTTTTTTTTTTT[1]	NC_000013.10:g.112755044_112755045insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

63 SubSNP, 34 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40297380	Oct 12, 2018 (152)
2	ABI	ss40359583	Oct 12, 2018 (152)
3	ABI	ss40361048	Oct 12, 2018 (152)
4	HGSV	ss82286875	Dec 14, 2007 (130)
5	HUMANGENOME_JCVI	ss95633701	Feb 05, 2009 (130)
6	PJP	ss294821242	Oct 12, 2018 (152)
7	PJP	ss294821243	Oct 12, 2018 (152)
8	PJP	ss294821244	Oct 12, 2018 (152)
9	SSMP	ss664161508	Apr 01, 2015 (144)
10	1000GENOMES	ss1373730781	Aug 21, 2014 (142)
11	EVA_UK10K_ALSPAC	ss1707958685	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1707958687	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1707958688	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1707958727	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1707958730	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1707958733	Apr 01, 2015 (144)
17	SWEGEN	ss3011743340	Nov 08, 2017 (151)
18	URBANLAB	ss3650143032	Oct 12, 2018 (152)
19	EVA_DECODE	ss3696170098	Jul 13, 2019 (153)
20	EVA_DECODE	ss3696170099	Jul 13, 2019 (153)
21	EVA_DECODE	ss3696170100	Jul 13, 2019 (153)
22	EVA_DECODE	ss3696170101	Jul 13, 2019 (153)
23	EVA_DECODE	ss3696170102	Jul 13, 2019 (153)
24	EVA_DECODE	ss3696170103	Jul 13, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3817343085	Jul 13, 2019 (153)
26	EVA	ss3833784403	Apr 27, 2020 (154)
27	GNOMAD	ss4273567324	Apr 26, 2021 (155)
28	GNOMAD	ss4273567325	Apr 26, 2021 (155)
29	GNOMAD	ss4273567326	Apr 26, 2021 (155)
30	GNOMAD	ss4273567327	Apr 26, 2021 (155)
31	GNOMAD	ss4273567328	Apr 26, 2021 (155)
32	GNOMAD	ss4273567329	Apr 26, 2021 (155)
33	GNOMAD	ss4273567330	Apr 26, 2021 (155)
34	GNOMAD	ss4273567331	Apr 26, 2021 (155)
35	GNOMAD	ss4273567332	Apr 26, 2021 (155)
36	GNOMAD	ss4273567333	Apr 26, 2021 (155)
37	GNOMAD	ss4273567334	Apr 26, 2021 (155)
38	GNOMAD	ss4273567335	Apr 26, 2021 (155)
39	GNOMAD	ss4273567336	Apr 26, 2021 (155)
40	GNOMAD	ss4273567337	Apr 26, 2021 (155)
41	GNOMAD	ss4273567338	Apr 26, 2021 (155)
42	GNOMAD	ss4273567339	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5211979722	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5211979723	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5211979724	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5211979725	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5211979726	Apr 26, 2021 (155)
48	1000G_HIGH_COVERAGE	ss5295273983	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5295273984	Oct 16, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5295273985	Oct 16, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5295273986	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5489484817	Oct 16, 2022 (156)
53	HUGCELL_USP	ss5489484818	Oct 16, 2022 (156)
54	HUGCELL_USP	ss5489484819	Oct 16, 2022 (156)
55	HUGCELL_USP	ss5489484820	Oct 16, 2022 (156)
56	HUGCELL_USP	ss5489484821	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5489484822	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5764400358	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5764400359	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5764400361	Oct 16, 2022 (156)
61	TOMMO_GENOMICS	ss5764400362	Oct 16, 2022 (156)
62	TOMMO_GENOMICS	ss5764400363	Oct 16, 2022 (156)
63	EVA	ss5926873139	Oct 16, 2022 (156)
64	1000Genomes	NC_000013.10 - 112755026	Oct 12, 2018 (152)
65	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 34968244 (NC_000013.10:112755025::TT 1308/3854) Row 34968245 (NC_000013.10:112755025::T 1635/3854) Row 34968246 (NC_000013.10:112755025::TTT 825/3854)	-	Oct 12, 2018 (152)
66	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 34968244 (NC_000013.10:112755025::TT 1308/3854) Row 34968245 (NC_000013.10:112755025::T 1635/3854) Row 34968246 (NC_000013.10:112755025::TTT 825/3854)	-	Oct 12, 2018 (152)
67	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 34968244 (NC_000013.10:112755025::TT 1308/3854) Row 34968245 (NC_000013.10:112755025::T 1635/3854) Row 34968246 (NC_000013.10:112755025::TTT 825/3854)	-	Oct 12, 2018 (152)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 443595839 (NC_000013.11:112100711::T 25260/107414) Row 443595840 (NC_000013.11:112100711::TT 9728/107508) Row 443595841 (NC_000013.11:112100711::TTT 22278/107326)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 69949029 (NC_000013.10:112755025::TTTT 46/16568) Row 69949030 (NC_000013.10:112755025::TTT 3919/16568) Row 69949031 (NC_000013.10:112755025::T 2027/16568)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 69949029 (NC_000013.10:112755025::TTTT 46/16568) Row 69949030 (NC_000013.10:112755025::TTT 3919/16568) Row 69949031 (NC_000013.10:112755025::T 2027/16568)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 69949029 (NC_000013.10:112755025::TTTT 46/16568) Row 69949030 (NC_000013.10:112755025::TTT 3919/16568) Row 69949031 (NC_000013.10:112755025::T 2027/16568)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 69949029 (NC_000013.10:112755025::TTTT 46/16568) Row 69949030 (NC_000013.10:112755025::TTT 3919/16568) Row 69949031 (NC_000013.10:112755025::T 2027/16568)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 69949029 (NC_000013.10:112755025::TTTT 46/16568) Row 69949030 (NC_000013.10:112755025::TTT 3919/16568) Row 69949031 (NC_000013.10:112755025::T 2027/16568)...	-	Apr 26, 2021 (155)
89	14KJPN Submission ignored due to conflicting rows: Row 98237462 (NC_000013.11:112100711::TTT 7128/28110) Row 98237463 (NC_000013.11:112100711::T 3820/28110) Row 98237465 (NC_000013.11:112100711::TTTT 58/28110)...	-	Oct 16, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 98237462 (NC_000013.11:112100711::TTT 7128/28110) Row 98237463 (NC_000013.11:112100711::T 3820/28110) Row 98237465 (NC_000013.11:112100711::TTTT 58/28110)...	-	Oct 16, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 98237462 (NC_000013.11:112100711::TTT 7128/28110) Row 98237463 (NC_000013.11:112100711::T 3820/28110) Row 98237465 (NC_000013.11:112100711::TTTT 58/28110)...	-	Oct 16, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 98237462 (NC_000013.11:112100711::TTT 7128/28110) Row 98237463 (NC_000013.11:112100711::T 3820/28110) Row 98237465 (NC_000013.11:112100711::TTTT 58/28110)...	-	Oct 16, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 98237462 (NC_000013.11:112100711::TTT 7128/28110) Row 98237463 (NC_000013.11:112100711::T 3820/28110) Row 98237465 (NC_000013.11:112100711::TTTT 58/28110)...	-	Oct 16, 2022 (156)
94	UK 10K study - Twins Submission ignored due to conflicting rows: Row 34968244 (NC_000013.10:112755025::TT 1273/3708) Row 34968245 (NC_000013.10:112755025::T 1535/3708) Row 34968246 (NC_000013.10:112755025::TTT 807/3708)	-	Oct 12, 2018 (152)
95	UK 10K study - Twins Submission ignored due to conflicting rows: Row 34968244 (NC_000013.10:112755025::TT 1273/3708) Row 34968245 (NC_000013.10:112755025::T 1535/3708) Row 34968246 (NC_000013.10:112755025::TTT 807/3708)	-	Oct 12, 2018 (152)
96	UK 10K study - Twins Submission ignored due to conflicting rows: Row 34968244 (NC_000013.10:112755025::TT 1273/3708) Row 34968245 (NC_000013.10:112755025::T 1535/3708) Row 34968246 (NC_000013.10:112755025::TTT 807/3708)	-	Oct 12, 2018 (152)
97	ALFA	NC_000013.11 - 112100712	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)
rs57739495	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4273567339	NC_000013.11:112100711:TTTTTT:	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
9735061483	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4273567338	NC_000013.11:112100711:TTTT:	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3011743340	NC_000013.10:112755025:TTT:	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3696170098, ss4273567337	NC_000013.11:112100711:TTT:	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
9735061483	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4273567336, ss5489484817	NC_000013.11:112100711:TT:	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
9735061483	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
62919364, ss1373730781	NC_000013.10:112755025:T:	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3817343085, ss4273567335, ss5489484821	NC_000013.11:112100711:T:	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9735061483	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3696170099	NC_000013.11:112100713:T:	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss294821244	NC_000013.9:111803045::T	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss664161508, ss1707958687, ss1707958730, ss3833784403, ss5211979724	NC_000013.10:112755025::T	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4273567324, ss5295273983, ss5489484818, ss5764400359	NC_000013.11:112100711::T	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
9735061483	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3696170100	NC_000013.11:112100714::T	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss40297380, ss40359583, ss40361048	NT_027140.6:251031::T	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss1707958685, ss1707958727, ss5211979725	NC_000013.10:112755025::TT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4273567325, ss5295273985, ss5489484819, ss5764400362, ss5926873139	NC_000013.11:112100711::TT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
9735061483	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3696170101	NC_000013.11:112100714::TT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss82286875	NT_027140.6:251050::TT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss294821242	NC_000013.9:111803027::TTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss294821243	NC_000013.9:111803043::TTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss1707958688, ss1707958733, ss5211979723	NC_000013.10:112755025::TTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3650143032, ss4273567326, ss5295273986, ss5489484820, ss5764400358	NC_000013.11:112100711::TTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
9735061483	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3696170102	NC_000013.11:112100714::TTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss95633701	NT_027140.6:251050::TTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5211979722	NC_000013.10:112755025::TTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4273567327, ss5295273984, ss5489484822, ss5764400361	NC_000013.11:112100711::TTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
9735061483	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3696170103	NC_000013.11:112100714::TTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5211979726	NC_000013.10:112755025::TTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4273567328, ss5764400363	NC_000013.11:112100711::TTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
9735061483	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4273567329	NC_000013.11:112100711::TTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9735061483	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4273567330	NC_000013.11:112100711::TTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4273567331	NC_000013.11:112100711::TTTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4273567332	NC_000013.11:112100711::TTTTTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4273567333	NC_000013.11:112100711::TTTTTTTTTT… NC_000013.11:112100711::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT	(self)
ss4273567334	NC_000013.11:112100711::TTTTTTTTTT… NC_000013.11:112100711::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000013.11:112100711:TTTTTTTTTTT… NC_000013.11:112100711:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs11420509

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.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11420509