Name: rs11295505
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.

rs11295505

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:39437286-39437297 (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)₇ / delTT / delT / dupT / du…
del(T)₇ / delTT / delT / dupT / dupTT
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.06032 (671/11124, ALFA)
delT=0.3724 (1865/5008, 1000G)
delT=0.1544 (595/3854, ALSPAC) (+ 3 more)
delT=0.1419 (526/3708, TWINSUK)
delT=0.206 (123/598, NorthernSweden)
delT=0.23 (9/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RPS16 : 2KB Upstream 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	11124	TTTTTTTTTTTT=0.93941	TTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.06032, TTTTTTTTTTTTT=0.00027, TTTTTTTTTTTTTT=0.00000	0.891887	0.012232	0.095881	32
European	Sub	9644	TTTTTTTTTTTT=0.9301	TTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0696, TTTTTTTTTTTTT=0.0003, TTTTTTTTTTTTTT=0.0000	0.875285	0.014111	0.110604	32
African	Sub	724	TTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	18	TTTTTTTTTTTT=1.00	TTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	706	TTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	40	TTTTTTTTTTTT=1.00	TTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	32	TTTTTTTTTTTT=1.00	TTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTT=1.0	TTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	66	TTTTTTTTTTTT=1.00	TTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	348	TTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	58	TTTTTTTTTTTT=1.00	TTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	244	TTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=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	11124	(T)₁₂=0.93941	del(T)₇=0.00000, delTT=0.00000, delT=0.06032, dupT=0.00027, dupTT=0.00000
Allele Frequency Aggregator	European	Sub	9644	(T)₁₂=0.9301	del(T)₇=0.0000, delTT=0.0000, delT=0.0696, dupT=0.0003, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	724	(T)₁₂=1.000	del(T)₇=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	348	(T)₁₂=1.000	del(T)₇=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	244	(T)₁₂=1.000	del(T)₇=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	66	(T)₁₂=1.00	del(T)₇=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	58	(T)₁₂=1.00	del(T)₇=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	40	(T)₁₂=1.00	del(T)₇=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₂=0.6276	delT=0.3724
1000Genomes	African	Sub	1322	(T)₁₂=0.4803	delT=0.5197
1000Genomes	East Asian	Sub	1008	(T)₁₂=0.5694	delT=0.4306
1000Genomes	Europe	Sub	1006	(T)₁₂=0.7813	delT=0.2187
1000Genomes	South Asian	Sub	978	(T)₁₂=0.654	delT=0.346
1000Genomes	American	Sub	694	(T)₁₂=0.732	delT=0.268
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₁₂=0.8456	delT=0.1544
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(T)₁₂=0.8581	delT=0.1419
Northern Sweden	ACPOP	Study-wide	598	(T)₁₂=0.794	delT=0.206
The Danish reference pan genome	Danish	Study-wide	40	(T)₁₂=0.78	delT=0.23

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.39437291_39437297del
GRCh38.p14 chr 19	NC_000019.10:g.39437296_39437297del
GRCh38.p14 chr 19	NC_000019.10:g.39437297del
GRCh38.p14 chr 19	NC_000019.10:g.39437297dup
GRCh38.p14 chr 19	NC_000019.10:g.39437296_39437297dup
GRCh37.p13 chr 19	NC_000019.9:g.39927931_39927937del
GRCh37.p13 chr 19	NC_000019.9:g.39927936_39927937del
GRCh37.p13 chr 19	NC_000019.9:g.39927937del
GRCh37.p13 chr 19	NC_000019.9:g.39927937dup
GRCh37.p13 chr 19	NC_000019.9:g.39927936_39927937dup

Gene: RPS16, ribosomal protein S16 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
RPS16 transcript variant 1	NM_001020.6:c.	N/A	Upstream Transcript Variant
RPS16 transcript variant 2	NM_001321111.2:c.	N/A	Upstream Transcript Variant
RPS16 transcript variant 3	NM_001363860.2:c.	N/A	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)₁₂=	del(T)₇	delTT	delT	dupT	dupTT
GRCh38.p14 chr 19	NC_000019.10:g.39437286_39437297=	NC_000019.10:g.39437291_39437297del	NC_000019.10:g.39437296_39437297del	NC_000019.10:g.39437297del	NC_000019.10:g.39437297dup	NC_000019.10:g.39437296_39437297dup
GRCh37.p13 chr 19	NC_000019.9:g.39927926_39927937=	NC_000019.9:g.39927931_39927937del	NC_000019.9:g.39927936_39927937del	NC_000019.9:g.39927937del	NC_000019.9:g.39927937dup	NC_000019.9:g.39927936_39927937dup

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#.

43 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	DEVINE_LAB	ss15171164	Mar 15, 2016 (147)
2	HGSV	ss81587337	Sep 08, 2015 (146)
3	BUSHMAN	ss193510823	Jul 04, 2010 (132)
4	GMI	ss289388318	May 04, 2012 (137)
5	PJP	ss294962881	May 09, 2011 (134)
6	BILGI_BIOE	ss666731997	Apr 25, 2013 (138)
7	1000GENOMES	ss1378147291	Aug 21, 2014 (142)
8	EVA_GENOME_DK	ss1575282743	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1709203081	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1709203365	Apr 01, 2015 (144)
11	HAMMER_LAB	ss1809306607	Sep 08, 2015 (146)
12	SWEGEN	ss3017467964	Nov 08, 2017 (151)
13	MCHAISSO	ss3063916234	Nov 08, 2017 (151)
14	EVA_DECODE	ss3702764186	Jul 13, 2019 (153)
15	EVA_DECODE	ss3702764187	Jul 13, 2019 (153)
16	ACPOP	ss3743037062	Jul 13, 2019 (153)
17	PACBIO	ss3788530929	Jul 13, 2019 (153)
18	PACBIO	ss3793441479	Jul 13, 2019 (153)
19	PACBIO	ss3798328276	Jul 13, 2019 (153)
20	KHV_HUMAN_GENOMES	ss3821310094	Jul 13, 2019 (153)
21	EVA	ss3835461275	Apr 27, 2020 (154)
22	KOGIC	ss3981344694	Apr 27, 2020 (154)
23	KOGIC	ss3981344695	Apr 27, 2020 (154)
24	GNOMAD	ss4331188760	Apr 27, 2021 (155)
25	GNOMAD	ss4331188761	Apr 27, 2021 (155)
26	GNOMAD	ss4331188762	Apr 27, 2021 (155)
27	GNOMAD	ss4331188763	Apr 27, 2021 (155)
28	GNOMAD	ss4331188764	Apr 27, 2021 (155)
29	TOMMO_GENOMICS	ss5227747775	Apr 27, 2021 (155)
30	TOMMO_GENOMICS	ss5227747776	Apr 27, 2021 (155)
31	TOMMO_GENOMICS	ss5227747777	Apr 27, 2021 (155)
32	1000G_HIGH_COVERAGE	ss5307239622	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5307239623	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5499766657	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5499766658	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5786377428	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5786377429	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5786377430	Oct 16, 2022 (156)
39	YY_MCH	ss5817599831	Oct 16, 2022 (156)
40	EVA	ss5840546439	Oct 16, 2022 (156)
41	EVA	ss5852289611	Oct 16, 2022 (156)
42	EVA	ss5928095797	Oct 16, 2022 (156)
43	EVA	ss5953802043	Oct 16, 2022 (156)
44	1000Genomes	NC_000019.9 - 39927926	Oct 12, 2018 (152)
45	The Avon Longitudinal Study of Parents and Children	NC_000019.9 - 39927926	Oct 12, 2018 (152)
46	The Danish reference pan genome	NC_000019.9 - 39927926	Apr 27, 2020 (154)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 539987462 (NC_000019.10:39437285::T 471/126976) Row 539987463 (NC_000019.10:39437285::TT 1/127082) Row 539987465 (NC_000019.10:39437285:T: 36148/126914)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 539987462 (NC_000019.10:39437285::T 471/126976) Row 539987463 (NC_000019.10:39437285::TT 1/127082) Row 539987465 (NC_000019.10:39437285:T: 36148/126914)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 539987462 (NC_000019.10:39437285::T 471/126976) Row 539987463 (NC_000019.10:39437285::TT 1/127082) Row 539987465 (NC_000019.10:39437285:T: 36148/126914)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 539987462 (NC_000019.10:39437285::T 471/126976) Row 539987463 (NC_000019.10:39437285::TT 1/127082) Row 539987465 (NC_000019.10:39437285:T: 36148/126914)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 539987462 (NC_000019.10:39437285::T 471/126976) Row 539987463 (NC_000019.10:39437285::TT 1/127082) Row 539987465 (NC_000019.10:39437285:T: 36148/126914)...	-	Apr 27, 2021 (155)
52	Korean Genome Project Submission ignored due to conflicting rows: Row 37722695 (NC_000019.10:39437285:T: 731/1832) Row 37722696 (NC_000019.10:39437286::T 40/1832)	-	Apr 27, 2020 (154)
53	Korean Genome Project Submission ignored due to conflicting rows: Row 37722695 (NC_000019.10:39437285:T: 731/1832) Row 37722696 (NC_000019.10:39437286::T 40/1832)	-	Apr 27, 2020 (154)
54	Northern Sweden	NC_000019.9 - 39927926	Jul 13, 2019 (153)
55	8.3KJPN Submission ignored due to conflicting rows: Row 85717082 (NC_000019.9:39927925:T: 5954/16756) Row 85717083 (NC_000019.9:39927925::T 96/16756) Row 85717084 (NC_000019.9:39927925:TT: 6/16756)	-	Apr 27, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 85717082 (NC_000019.9:39927925:T: 5954/16756) Row 85717083 (NC_000019.9:39927925::T 96/16756) Row 85717084 (NC_000019.9:39927925:TT: 6/16756)	-	Apr 27, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 85717082 (NC_000019.9:39927925:T: 5954/16756) Row 85717083 (NC_000019.9:39927925::T 96/16756) Row 85717084 (NC_000019.9:39927925:TT: 6/16756)	-	Apr 27, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 120214532 (NC_000019.10:39437285:T: 8745/27100) Row 120214533 (NC_000019.10:39437285::T 139/27100) Row 120214534 (NC_000019.10:39437285:TT: 5/27100)	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 120214532 (NC_000019.10:39437285:T: 8745/27100) Row 120214533 (NC_000019.10:39437285::T 139/27100) Row 120214534 (NC_000019.10:39437285:TT: 5/27100)	-	Oct 16, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 120214532 (NC_000019.10:39437285:T: 8745/27100) Row 120214533 (NC_000019.10:39437285::T 139/27100) Row 120214534 (NC_000019.10:39437285:TT: 5/27100)	-	Oct 16, 2022 (156)
61	UK 10K study - Twins	NC_000019.9 - 39927926	Oct 12, 2018 (152)
62	ALFA	NC_000019.10 - 39437286	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)
rs58819570	May 11, 2012 (137)
rs869104571	Jul 19, 2016 (147)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4331188764	NC_000019.10:39437285:TTTTTTT:	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTT	(self)
8466656072	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTT	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTT	(self)
ss5227747777	NC_000019.9:39927925:TT:	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4331188763, ss5786377430	NC_000019.10:39437285:TT:	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTT	(self)
8466656072	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTT	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss289388318, ss294962881	NC_000019.8:44619765:T:	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss81587337	NC_000019.8:44619776:T:	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
76562753, 42406106, 633785, 16321927, 42406106, ss666731997, ss1378147291, ss1575282743, ss1709203081, ss1709203365, ss1809306607, ss3017467964, ss3743037062, ss3788530929, ss3793441479, ss3798328276, ss3835461275, ss5227747775, ss5840546439, ss5953802043	NC_000019.9:39927925:T:	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3063916234, ss3702764186, ss3821310094, ss3981344694, ss4331188762, ss5307239622, ss5499766657, ss5786377428, ss5817599831, ss5852289611, ss5928095797	NC_000019.10:39437285:T:	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
8466656072	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTT	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss15171164	NT_011109.16:12196143:T:	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss193510823	NT_011109.17:12196411:T:	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss5227747776	NC_000019.9:39927925::T	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4331188760, ss5307239623, ss5499766658, ss5786377429	NC_000019.10:39437285::T	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
8466656072	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3702764187, ss3981344695	NC_000019.10:39437286::T	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4331188761	NC_000019.10:39437285::TT	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
8466656072	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000019.10:39437285:TTTTTTTTTTTT… NC_000019.10:39437285:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(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 rs11295505

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

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