Name: rs111854110
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.

rs111854110

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:31111840-31111852 (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
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.09811 (2353/23983, ALFA)

Clinical Significance: Reported in ClinVar
Gene : Consequence: WRN : 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	HTRZ	HWEP
Total	Global	23983	TTTTTTTTTTTTT=0.85506	TTTTTTTTTTT=0.00233, TTTTTTTTTTTT=0.09811, TTTTTTTTTTTTTT=0.04391, TTTTTTTTTTTTTTT=0.00058	0.783677	0.216323	32
European	Sub	18128	TTTTTTTTTTTTT=0.87307	TTTTTTTTTTT=0.00182, TTTTTTTTTTTT=0.08639, TTTTTTTTTTTTTT=0.03828, TTTTTTTTTTTTTTT=0.00044	0.811982	0.188018	32
African	Sub	2205	TTTTTTTTTTTTT=0.8875	TTTTTTTTTTT=0.0018, TTTTTTTTTTTT=0.0834, TTTTTTTTTTTTTT=0.0272, TTTTTTTTTTTTTTT=0.0000	0.824663	0.175337	6
African Others	Sub	74	TTTTTTTTTTTTT=0.96	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.03, TTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTT=0.00	0.944444	0.055556	0
African American	Sub	2131	TTTTTTTTTTTTT=0.8850	TTTTTTTTTTT=0.0019, TTTTTTTTTTTT=0.0854, TTTTTTTTTTTTTT=0.0277, TTTTTTTTTTTTTTT=0.0000	0.820359	0.179641	6
Asian	Sub	164	TTTTTTTTTTTTT=0.872	TTTTTTTTTTT=0.006, TTTTTTTTTTTT=0.079, TTTTTTTTTTTTTT=0.043, TTTTTTTTTTTTTTT=0.000	0.824324	0.175676	0
East Asian	Sub	110	TTTTTTTTTTTTT=0.927	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.045, TTTTTTTTTTTTTT=0.027, TTTTTTTTTTTTTTT=0.000	0.903846	0.096154	0
Other Asian	Sub	54	TTTTTTTTTTTTT=0.76	TTTTTTTTTTT=0.02, TTTTTTTTTTTT=0.15, TTTTTTTTTTTTTT=0.07, TTTTTTTTTTTTTTT=0.00	0.636364	0.363636	1
Latin American 1	Sub	130	TTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	N/A
Latin American 2	Sub	576	TTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	N/A
South Asian	Sub	92	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
Other	Sub	2688	TTTTTTTTTTTTT=0.6629	TTTTTTTTTTT=0.0067, TTTTTTTTTTTT=0.2195, TTTTTTTTTTTTTT=0.1086, TTTTTTTTTTTTTTT=0.0022	0.42607	0.57393	32

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	23983	(T)₁₃=0.85506	delTT=0.00233, delT=0.09811, dupT=0.04391, dupTT=0.00058
Allele Frequency Aggregator	European	Sub	18128	(T)₁₃=0.87307	delTT=0.00182, delT=0.08639, dupT=0.03828, dupTT=0.00044
Allele Frequency Aggregator	Other	Sub	2688	(T)₁₃=0.6629	delTT=0.0067, delT=0.2195, dupT=0.1086, dupTT=0.0022
Allele Frequency Aggregator	African	Sub	2205	(T)₁₃=0.8875	delTT=0.0018, delT=0.0834, dupT=0.0272, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	576	(T)₁₃=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Asian	Sub	164	(T)₁₃=0.872	delTT=0.006, delT=0.079, dupT=0.043, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	130	(T)₁₃=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	South Asian	Sub	92	(T)₁₃=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00

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 8	NC_000008.11:g.31111850_31111852del
GRCh38.p14 chr 8	NC_000008.11:g.31111851_31111852del
GRCh38.p14 chr 8	NC_000008.11:g.31111852del
GRCh38.p14 chr 8	NC_000008.11:g.31111852dup
GRCh38.p14 chr 8	NC_000008.11:g.31111851_31111852dup
GRCh38.p14 chr 8	NC_000008.11:g.31111850_31111852dup
GRCh37.p13 chr 8	NC_000008.10:g.30969366_30969368del
GRCh37.p13 chr 8	NC_000008.10:g.30969367_30969368del
GRCh37.p13 chr 8	NC_000008.10:g.30969368del
GRCh37.p13 chr 8	NC_000008.10:g.30969368dup
GRCh37.p13 chr 8	NC_000008.10:g.30969367_30969368dup
GRCh37.p13 chr 8	NC_000008.10:g.30969366_30969368dup
WRN RefSeqGene (LRG_524)	NG_008870.1:g.83589_83591del
WRN RefSeqGene (LRG_524)	NG_008870.1:g.83590_83591del
WRN RefSeqGene (LRG_524)	NG_008870.1:g.83591del
WRN RefSeqGene (LRG_524)	NG_008870.1:g.83591dup
WRN RefSeqGene (LRG_524)	NG_008870.1:g.83590_83591dup
WRN RefSeqGene (LRG_524)	NG_008870.1:g.83589_83591dup

Gene: WRN, WRN RecQ like helicase (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
WRN transcript	NM_000553.6:c.2273+51_227… NM_000553.6:c.2273+51_2273+53del	N/A	Intron Variant
WRN transcript variant X1	XM_011544639.4:c.2192+51_… XM_011544639.4:c.2192+51_2192+53del	N/A	Intron Variant
WRN transcript variant X5	XM_011544640.2:c.674+51_6… XM_011544640.2:c.674+51_674+53del	N/A	Intron Variant
WRN transcript variant X2	XR_949470.4:n.	N/A	Intron Variant
WRN transcript variant X3	XR_949471.4:n.	N/A	Intron Variant
WRN transcript variant X4	XR_949472.4: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.

Allele: dupT (allele ID: 1334651 )

ClinVar Accession	Disease Names	Clinical Significance
RCV001843608.1	not provided	Benign

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)₁₃=	delTTT	delTT	delT	dupT	dupTT	dupTTT
GRCh38.p14 chr 8	NC_000008.11:g.31111840_31111852=	NC_000008.11:g.31111850_31111852del	NC_000008.11:g.31111851_31111852del	NC_000008.11:g.31111852del	NC_000008.11:g.31111852dup	NC_000008.11:g.31111851_31111852dup	NC_000008.11:g.31111850_31111852dup
GRCh37.p13 chr 8	NC_000008.10:g.30969356_30969368=	NC_000008.10:g.30969366_30969368del	NC_000008.10:g.30969367_30969368del	NC_000008.10:g.30969368del	NC_000008.10:g.30969368dup	NC_000008.10:g.30969367_30969368dup	NC_000008.10:g.30969366_30969368dup
WRN RefSeqGene (LRG_524)	NG_008870.1:g.83579_83591=	NG_008870.1:g.83589_83591del	NG_008870.1:g.83590_83591del	NG_008870.1:g.83591del	NG_008870.1:g.83591dup	NG_008870.1:g.83590_83591dup	NG_008870.1:g.83589_83591dup
WRN transcript	NM_000553.4:c.2273+41=	NM_000553.4:c.2273+51_2273+53del	NM_000553.4:c.2273+52_2273+53del	NM_000553.4:c.2273+53del	NM_000553.4:c.2273+53dup	NM_000553.4:c.2273+52_2273+53dup	NM_000553.4:c.2273+51_2273+53dup
WRN transcript	NM_000553.6:c.2273+41=	NM_000553.6:c.2273+51_2273+53del	NM_000553.6:c.2273+52_2273+53del	NM_000553.6:c.2273+53del	NM_000553.6:c.2273+53dup	NM_000553.6:c.2273+52_2273+53dup	NM_000553.6:c.2273+51_2273+53dup
WRN transcript variant X1	XM_005273632.1:c.2192+41=	XM_005273632.1:c.2192+51_2192+53del	XM_005273632.1:c.2192+52_2192+53del	XM_005273632.1:c.2192+53del	XM_005273632.1:c.2192+53dup	XM_005273632.1:c.2192+52_2192+53dup	XM_005273632.1:c.2192+51_2192+53dup
WRN transcript variant X1	XM_011544639.4:c.2192+41=	XM_011544639.4:c.2192+51_2192+53del	XM_011544639.4:c.2192+52_2192+53del	XM_011544639.4:c.2192+53del	XM_011544639.4:c.2192+53dup	XM_011544639.4:c.2192+52_2192+53dup	XM_011544639.4:c.2192+51_2192+53dup
WRN transcript variant X5	XM_011544640.2:c.674+41=	XM_011544640.2:c.674+51_674+53del	XM_011544640.2:c.674+52_674+53del	XM_011544640.2:c.674+53del	XM_011544640.2:c.674+53dup	XM_011544640.2:c.674+52_674+53dup	XM_011544640.2:c.674+51_674+53dup

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#.

26 SubSNP, 15 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	BUSHMAN	ss193970327	Jul 04, 2010 (132)
2	SSIP	ss947216627	Aug 21, 2014 (142)
3	EVA_EXAC	ss1711884501	Apr 01, 2015 (144)
4	EVA_EXAC	ss1711884502	Apr 01, 2015 (144)
5	EVA_EXAC	ss1711884503	Jan 10, 2018 (151)
6	EVA_EXAC	ss1711884504	Apr 01, 2015 (144)
7	EVA_EXAC	ss1711884505	Apr 01, 2015 (144)
8	MCHAISSO	ss3066195855	Nov 08, 2017 (151)
9	FSA-LAB	ss3984397097	Apr 26, 2021 (155)
10	EVA	ss3986419863	Apr 26, 2021 (155)
11	GNOMAD	ss4181776149	Apr 26, 2021 (155)
12	GNOMAD	ss4181776150	Apr 26, 2021 (155)
13	GNOMAD	ss4181776152	Apr 26, 2021 (155)
14	GNOMAD	ss4181776153	Apr 26, 2021 (155)
15	GNOMAD	ss4181776154	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5188036189	Apr 26, 2021 (155)
17	TOMMO_GENOMICS	ss5188036190	Apr 26, 2021 (155)
18	EVA	ss5237200977	Apr 26, 2021 (155)
19	1000G_HIGH_COVERAGE	ss5276629504	Oct 16, 2022 (156)
20	1000G_HIGH_COVERAGE	ss5276629505	Oct 16, 2022 (156)
21	HUGCELL_USP	ss5473252711	Oct 16, 2022 (156)
22	HUGCELL_USP	ss5473252712	Oct 16, 2022 (156)
23	TOMMO_GENOMICS	ss5729764348	Oct 16, 2022 (156)
24	TOMMO_GENOMICS	ss5729764349	Oct 16, 2022 (156)
25	EVA	ss5800059347	Oct 16, 2022 (156)
26	EVA	ss5935923568	Oct 16, 2022 (156)
27	ExAC Submission ignored due to conflicting rows: Row 9254395 (NC_000008.10:30969355:TTT: 1/61446) Row 9254396 (NC_000008.10:30969355:TT: 159/61446) Row 9254397 (NC_000008.10:30969355:T: 17418/61446) Row 9254398 (NC_000008.10:30969355::T 3471/61446) Row 9254399 (NC_000008.10:30969355::TT 16/61446)	-	Oct 12, 2018 (152)
28	ExAC Submission ignored due to conflicting rows: Row 9254395 (NC_000008.10:30969355:TTT: 1/61446) Row 9254396 (NC_000008.10:30969355:TT: 159/61446) Row 9254397 (NC_000008.10:30969355:T: 17418/61446) Row 9254398 (NC_000008.10:30969355::T 3471/61446) Row 9254399 (NC_000008.10:30969355::TT 16/61446)	-	Oct 12, 2018 (152)
29	ExAC Submission ignored due to conflicting rows: Row 9254395 (NC_000008.10:30969355:TTT: 1/61446) Row 9254396 (NC_000008.10:30969355:TT: 159/61446) Row 9254397 (NC_000008.10:30969355:T: 17418/61446) Row 9254398 (NC_000008.10:30969355::T 3471/61446) Row 9254399 (NC_000008.10:30969355::TT 16/61446)	-	Oct 12, 2018 (152)
30	ExAC Submission ignored due to conflicting rows: Row 9254395 (NC_000008.10:30969355:TTT: 1/61446) Row 9254396 (NC_000008.10:30969355:TT: 159/61446) Row 9254397 (NC_000008.10:30969355:T: 17418/61446) Row 9254398 (NC_000008.10:30969355::T 3471/61446) Row 9254399 (NC_000008.10:30969355::TT 16/61446)	-	Oct 12, 2018 (152)
31	ExAC Submission ignored due to conflicting rows: Row 9254395 (NC_000008.10:30969355:TTT: 1/61446) Row 9254396 (NC_000008.10:30969355:TT: 159/61446) Row 9254397 (NC_000008.10:30969355:T: 17418/61446) Row 9254398 (NC_000008.10:30969355::T 3471/61446) Row 9254399 (NC_000008.10:30969355::TT 16/61446)	-	Oct 12, 2018 (152)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291632291 (NC_000008.11:31111839::T 3825/131094) Row 291632292 (NC_000008.11:31111839::TT 9/131178) Row 291632294 (NC_000008.11:31111839:T: 6915/130838)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291632291 (NC_000008.11:31111839::T 3825/131094) Row 291632292 (NC_000008.11:31111839::TT 9/131178) Row 291632294 (NC_000008.11:31111839:T: 6915/130838)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291632291 (NC_000008.11:31111839::T 3825/131094) Row 291632292 (NC_000008.11:31111839::TT 9/131178) Row 291632294 (NC_000008.11:31111839:T: 6915/130838)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291632291 (NC_000008.11:31111839::T 3825/131094) Row 291632292 (NC_000008.11:31111839::TT 9/131178) Row 291632294 (NC_000008.11:31111839:T: 6915/130838)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291632291 (NC_000008.11:31111839::T 3825/131094) Row 291632292 (NC_000008.11:31111839::TT 9/131178) Row 291632294 (NC_000008.11:31111839:T: 6915/130838)...	-	Apr 26, 2021 (155)
37	8.3KJPN Submission ignored due to conflicting rows: Row 46005496 (NC_000008.10:30969355:T: 31/16760) Row 46005497 (NC_000008.10:30969355::T 43/16760)	-	Apr 26, 2021 (155)
38	8.3KJPN Submission ignored due to conflicting rows: Row 46005496 (NC_000008.10:30969355:T: 31/16760) Row 46005497 (NC_000008.10:30969355::T 43/16760)	-	Apr 26, 2021 (155)
39	14KJPN Submission ignored due to conflicting rows: Row 63601452 (NC_000008.11:31111839:T: 37/28258) Row 63601453 (NC_000008.11:31111839::T 73/28258)	-	Oct 16, 2022 (156)
40	14KJPN Submission ignored due to conflicting rows: Row 63601452 (NC_000008.11:31111839:T: 37/28258) Row 63601453 (NC_000008.11:31111839::T 73/28258)	-	Oct 16, 2022 (156)
41	ALFA	NC_000008.11 - 31111840	Apr 26, 2021 (155)
42	ClinVar	RCV001843608.1	Oct 16, 2022 (156)

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)
rs796570612	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss1711884505	NC_000008.10:30969355:TTT:	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4181776154	NC_000008.11:31111839:TTT:	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss1711884503, ss3984397097	NC_000008.10:30969355:TT:	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4181776153	NC_000008.11:31111839:TT:	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
3971264224	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTT	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss1711884501, ss3986419863, ss5188036189, ss5800059347	NC_000008.10:30969355:T:	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3066195855, ss4181776152, ss5276629504, ss5473252712, ss5729764348	NC_000008.11:31111839:T:	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
3971264224	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss193970327	NT_167187.2:18827494:T:	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss1711884502, ss5188036190	NC_000008.10:30969355::T	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss947216627	NC_000008.10:30969356::T	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4181776149, ss5237200977, ss5276629505, ss5473252711, ss5729764349	NC_000008.11:31111839::T	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
RCV001843608.1, 3971264224	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss1711884504	NC_000008.10:30969355::TT	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4181776150	NC_000008.11:31111839::TT	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3971264224	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5935923568	NC_000008.10:30969355::TTT	NC_000008.11:31111839:TTTTTTTTTTTT… NC_000008.11:31111839:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs111854110

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

rs111854110