Name: rs11419805
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.

rs11419805

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chrX:39310818-39310832 (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: delTTT / delTT / delT / dupT / dup…
delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.07958 (833/10468, ALFA)
dupT=0.3030 (1144/3775, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC01281 : 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	10468	TTTTTTTTTTTTTTT=0.89683	TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00678, TTTTTTTTTTTTTTTT=0.07958, TTTTTTTTTTTTTTTTT=0.01672, TTTTTTTTTTTTTTTTTT=0.00010, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000	0.893613	0.052205	0.054182	32
European	Sub	8500	TTTTTTTTTTTTTTT=0.8732	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0084, TTTTTTTTTTTTTTTT=0.0980, TTTTTTTTTTTTTTTTT=0.0204, TTTTTTTTTTTTTTTTTT=0.0001, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	0.867943	0.064801	0.067256	32
African	Sub	1302	TTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	62	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1240	TTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	40	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	24	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	68	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	258	TTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	38	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	262	TTTTTTTTTTTTTTT=0.992	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.008, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	10468	(T)₁₅=0.89683	delTT=0.00000, delT=0.00678, dupT=0.07958, dupTT=0.01672, dupTTT=0.00010, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00000, dup(T)₇=0.00000
Allele Frequency Aggregator	European	Sub	8500	(T)₁₅=0.8732	delTT=0.0000, delT=0.0084, dupT=0.0980, dupTT=0.0204, dupTTT=0.0001, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000
Allele Frequency Aggregator	African	Sub	1302	(T)₁₅=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000
Allele Frequency Aggregator	Other	Sub	262	(T)₁₅=0.992	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.008, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 2	Sub	258	(T)₁₅=1.000	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, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	68	(T)₁₅=1.00	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, dup(T)₇=0.00
Allele Frequency Aggregator	Asian	Sub	40	(T)₁₅=1.00	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, dup(T)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	38	(T)₁₅=1.00	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, dup(T)₇=0.00
1000Genomes	Global	Study-wide	3775	- No frequency provided	dupT=0.3030
1000Genomes	African	Sub	1003	- No frequency provided	dupT=0.2722
1000Genomes	Europe	Sub	766	- No frequency provided	dupT=0.257
1000Genomes	East Asian	Sub	764	- No frequency provided	dupT=0.317
1000Genomes	South Asian	Sub	718	- No frequency provided	dupT=0.368
1000Genomes	American	Sub	524	- No frequency provided	dupT=0.321

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 X	NC_000023.11:g.39310830_39310832del
GRCh38.p14 chr X	NC_000023.11:g.39310831_39310832del
GRCh38.p14 chr X	NC_000023.11:g.39310832del
GRCh38.p14 chr X	NC_000023.11:g.39310832dup
GRCh38.p14 chr X	NC_000023.11:g.39310831_39310832dup
GRCh38.p14 chr X	NC_000023.11:g.39310830_39310832dup
GRCh38.p14 chr X	NC_000023.11:g.39310829_39310832dup
GRCh38.p14 chr X	NC_000023.11:g.39310828_39310832dup
GRCh38.p14 chr X	NC_000023.11:g.39310827_39310832dup
GRCh38.p14 chr X	NC_000023.11:g.39310826_39310832dup
GRCh37.p13 chr X	NC_000023.10:g.39170084_39170086del
GRCh37.p13 chr X	NC_000023.10:g.39170085_39170086del
GRCh37.p13 chr X	NC_000023.10:g.39170086del
GRCh37.p13 chr X	NC_000023.10:g.39170086dup
GRCh37.p13 chr X	NC_000023.10:g.39170085_39170086dup
GRCh37.p13 chr X	NC_000023.10:g.39170084_39170086dup
GRCh37.p13 chr X	NC_000023.10:g.39170083_39170086dup
GRCh37.p13 chr X	NC_000023.10:g.39170082_39170086dup
GRCh37.p13 chr X	NC_000023.10:g.39170081_39170086dup
GRCh37.p13 chr X	NC_000023.10:g.39170080_39170086dup

Gene: LINC01281, long intergenic non-protein coding RNA 1281 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC01281 transcript	NR_038968.1:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₁₅=	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇
GRCh38.p14 chr X	NC_000023.11:g.39310818_39310832=	NC_000023.11:g.39310830_39310832del	NC_000023.11:g.39310831_39310832del	NC_000023.11:g.39310832del	NC_000023.11:g.39310832dup	NC_000023.11:g.39310831_39310832dup	NC_000023.11:g.39310830_39310832dup	NC_000023.11:g.39310829_39310832dup	NC_000023.11:g.39310828_39310832dup	NC_000023.11:g.39310827_39310832dup	NC_000023.11:g.39310826_39310832dup
GRCh37.p13 chr X	NC_000023.10:g.39170072_39170086=	NC_000023.10:g.39170084_39170086del	NC_000023.10:g.39170085_39170086del	NC_000023.10:g.39170086del	NC_000023.10:g.39170086dup	NC_000023.10:g.39170085_39170086dup	NC_000023.10:g.39170084_39170086dup	NC_000023.10:g.39170083_39170086dup	NC_000023.10:g.39170082_39170086dup	NC_000023.10:g.39170081_39170086dup	NC_000023.10:g.39170080_39170086dup

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#.

38 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss43707073	Mar 14, 2006 (126)
2	ABI	ss43708349	Dec 03, 2013 (142)
3	HGSV	ss80917614	Dec 04, 2013 (142)
4	BCMHGSC_JDW	ss103791994	Mar 15, 2016 (147)
5	PJP	ss295451283	May 09, 2011 (134)
6	TISHKOFF	ss566688862	Apr 25, 2013 (138)
7	SSMP	ss664565537	Apr 01, 2015 (144)
8	1000GENOMES	ss1554154432	Apr 01, 2015 (144)
9	SYSTEMSBIOZJU	ss2629692759	Nov 08, 2017 (151)
10	SWEGEN	ss3019862283	Nov 08, 2017 (151)
11	MCHAISSO	ss3064365765	Nov 08, 2017 (151)
12	URBANLAB	ss3651266514	Oct 12, 2018 (152)
13	KHV_HUMAN_GENOMES	ss3822926710	Jul 13, 2019 (153)
14	EVA	ss3836149592	Apr 27, 2020 (154)
15	GNOMAD	ss4370355145	Apr 27, 2021 (155)
16	GNOMAD	ss4370355146	Apr 27, 2021 (155)
17	GNOMAD	ss4370355147	Apr 27, 2021 (155)
18	GNOMAD	ss4370355148	Apr 27, 2021 (155)
19	GNOMAD	ss4370355149	Apr 27, 2021 (155)
20	GNOMAD	ss4370355150	Apr 27, 2021 (155)
21	GNOMAD	ss4370355151	Apr 27, 2021 (155)
22	GNOMAD	ss4370355152	Apr 27, 2021 (155)
23	GNOMAD	ss4370355153	Apr 27, 2021 (155)
24	TOMMO_GENOMICS	ss5234171312	Apr 27, 2021 (155)
25	TOMMO_GENOMICS	ss5234171313	Apr 27, 2021 (155)
26	TOMMO_GENOMICS	ss5234171314	Apr 27, 2021 (155)
27	1000G_HIGH_COVERAGE	ss5312317050	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5312317051	Oct 16, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5312317052	Oct 16, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5312317053	Oct 16, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5312317054	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5504011678	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5504011679	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5504011680	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5504011681	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5795787905	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5795787906	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5795787907	Oct 16, 2022 (156)
39	1000Genomes	NC_000023.10 - 39170072	Oct 12, 2018 (152)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 578995908 (NC_000023.11:39310817::T 20938/91293) Row 578995909 (NC_000023.11:39310817::TT 7234/91400) Row 578995910 (NC_000023.11:39310817::TTT 160/91449)...	-	Apr 27, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 578995908 (NC_000023.11:39310817::T 20938/91293) Row 578995909 (NC_000023.11:39310817::TT 7234/91400) Row 578995910 (NC_000023.11:39310817::TTT 160/91449)...	-	Apr 27, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 578995908 (NC_000023.11:39310817::T 20938/91293) Row 578995909 (NC_000023.11:39310817::TT 7234/91400) Row 578995910 (NC_000023.11:39310817::TTT 160/91449)...	-	Apr 27, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 578995908 (NC_000023.11:39310817::T 20938/91293) Row 578995909 (NC_000023.11:39310817::TT 7234/91400) Row 578995910 (NC_000023.11:39310817::TTT 160/91449)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 578995908 (NC_000023.11:39310817::T 20938/91293) Row 578995909 (NC_000023.11:39310817::TT 7234/91400) Row 578995910 (NC_000023.11:39310817::TTT 160/91449)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 578995908 (NC_000023.11:39310817::T 20938/91293) Row 578995909 (NC_000023.11:39310817::TT 7234/91400) Row 578995910 (NC_000023.11:39310817::TTT 160/91449)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 578995908 (NC_000023.11:39310817::T 20938/91293) Row 578995909 (NC_000023.11:39310817::TT 7234/91400) Row 578995910 (NC_000023.11:39310817::TTT 160/91449)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 578995908 (NC_000023.11:39310817::T 20938/91293) Row 578995909 (NC_000023.11:39310817::TT 7234/91400) Row 578995910 (NC_000023.11:39310817::TTT 160/91449)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 578995908 (NC_000023.11:39310817::T 20938/91293) Row 578995909 (NC_000023.11:39310817::TT 7234/91400) Row 578995910 (NC_000023.11:39310817::TTT 160/91449)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 578995908 (NC_000023.11:39310817::T 20938/91293) Row 578995909 (NC_000023.11:39310817::TT 7234/91400) Row 578995910 (NC_000023.11:39310817::TTT 160/91449)...	-	Apr 27, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 92140619 (NC_000023.10:39170071::T 5777/12770) Row 92140620 (NC_000023.10:39170071:T: 112/12770) Row 92140621 (NC_000023.10:39170071::TT 365/12770)	-	Apr 27, 2021 (155)
51	8.3KJPN Submission ignored due to conflicting rows: Row 92140619 (NC_000023.10:39170071::T 5777/12770) Row 92140620 (NC_000023.10:39170071:T: 112/12770) Row 92140621 (NC_000023.10:39170071::TT 365/12770)	-	Apr 27, 2021 (155)
52	8.3KJPN Submission ignored due to conflicting rows: Row 92140619 (NC_000023.10:39170071::T 5777/12770) Row 92140620 (NC_000023.10:39170071:T: 112/12770) Row 92140621 (NC_000023.10:39170071::TT 365/12770)	-	Apr 27, 2021 (155)
53	14KJPN Submission ignored due to conflicting rows: Row 129625009 (NC_000023.11:39310817::T 10203/22211) Row 129625010 (NC_000023.11:39310817::TT 623/22211) Row 129625011 (NC_000023.11:39310817:T: 184/22211)	-	Oct 16, 2022 (156)
54	14KJPN Submission ignored due to conflicting rows: Row 129625009 (NC_000023.11:39310817::T 10203/22211) Row 129625010 (NC_000023.11:39310817::TT 623/22211) Row 129625011 (NC_000023.11:39310817:T: 184/22211)	-	Oct 16, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 129625009 (NC_000023.11:39310817::T 10203/22211) Row 129625010 (NC_000023.11:39310817::TT 623/22211) Row 129625011 (NC_000023.11:39310817:T: 184/22211)	-	Oct 16, 2022 (156)
56	ALFA	NC_000023.11 - 39310818	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)
rs56826712	May 26, 2008 (130)
rs374362422	May 15, 2013 (138)
rs79426889	Oct 12, 2011 (135)
rs397692172	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4370355153	NC_000023.11:39310817:TTT:	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss103791994	NT_079573.4:2021827:TTT:	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4370355152	NC_000023.11:39310817:TT:	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11346309011	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3019862283, ss5234171313	NC_000023.10:39170071:T:	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3064365765, ss5312317051, ss5504011680, ss5795787907	NC_000023.11:39310817:T:	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11346309011	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss43707073	NT_079573.4:2021829:T:	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss295451283	NC_000023.9:39055030::T	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
82132088, ss664565537, ss1554154432, ss2629692759, ss3836149592, ss5234171312	NC_000023.10:39170071::T	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss566688862	NC_000023.10:39170086::T	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3651266514, ss3822926710, ss4370355145, ss5312317050, ss5504011678, ss5795787905	NC_000023.11:39310817::T	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
11346309011	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss43708349, ss80917614	NT_079573.4:2021830::T	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5234171314	NC_000023.10:39170071::TT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4370355146, ss5312317052, ss5504011679, ss5795787906	NC_000023.11:39310817::TT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
11346309011	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4370355147, ss5312317054, ss5504011681	NC_000023.11:39310817::TTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
11346309011	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4370355148	NC_000023.11:39310817::TTTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
11346309011	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4370355149	NC_000023.11:39310817::TTTTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
11346309011	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4370355150, ss5312317053	NC_000023.11:39310817::TTTTTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
11346309011	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4370355151	NC_000023.11:39310817::TTTTTTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
11346309011	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:39310817:TTTTTTTTTTTT… NC_000023.11:39310817:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(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 rs11419805

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11419805