Name: rs35022195
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.

rs35022195

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:62346674-62346685 (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: delTT / delT / dupT / dupTT / dupT…
delTT / delT / dupT / dupTT / dupTTT / dup(T)₅
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1898 (1384/7292, ALFA)
delTT=0.1234 (396/3208, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC105371936 : 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	7292	TTTTTTTTTTTT=0.7457	TTTTTTTTTT=0.0618, TTTTTTTTTTT=0.0001, TTTTTTTTTTTTT=0.1898, TTTTTTTTTTTTTT=0.0025, TTTTTTTTTTTTTTT=0.0000	0.6961	0.082995	0.220905	32
European	Sub	6082	TTTTTTTTTTTT=0.6960	TTTTTTTTTT=0.0740, TTTTTTTTTTT=0.0002, TTTTTTTTTTTTT=0.2269, TTTTTTTTTTTTTT=0.0030, TTTTTTTTTTTTTTT=0.0000	0.626682	0.102268	0.27105	32
African	Sub	960	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	42	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	918	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	16	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	10	TTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	6	TTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	40	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	74	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	24	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	96	TTTTTTTTTTTT=0.95	TTTTTTTTTT=0.01, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.04, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	0.93617	0.0	0.06383	0

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	7292	(T)₁₂=0.7457	delTT=0.0618, delT=0.0001, dupT=0.1898, dupTT=0.0025, dupTTT=0.0000
Allele Frequency Aggregator	European	Sub	6082	(T)₁₂=0.6960	delTT=0.0740, delT=0.0002, dupT=0.2269, dupTT=0.0030, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	960	(T)₁₂=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	96	(T)₁₂=0.95	delTT=0.01, delT=0.00, dupT=0.04, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Latin American 2	Sub	74	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	40	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	24	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Asian	Sub	16	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
1000Genomes	Global	Study-wide	3208	(T)₁₂=0.8766	delTT=0.1234
1000Genomes	African	Sub	1006	(T)₁₂=0.9274	delTT=0.0726
1000Genomes	South Asian	Sub	667	(T)₁₂=0.841	delTT=0.159
1000Genomes	Europe	Sub	644	(T)₁₂=0.769	delTT=0.231
1000Genomes	East Asian	Sub	548	(T)₁₂=0.985	delTT=0.015
1000Genomes	American	Sub	343	(T)₁₂=0.825	delTT=0.175

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 17	NC_000017.11:g.62346684_62346685del
GRCh38.p14 chr 17	NC_000017.11:g.62346685del
GRCh38.p14 chr 17	NC_000017.11:g.62346685dup
GRCh38.p14 chr 17	NC_000017.11:g.62346684_62346685dup
GRCh38.p14 chr 17	NC_000017.11:g.62346683_62346685dup
GRCh38.p14 chr 17	NC_000017.11:g.62346681_62346685dup
GRCh37.p13 chr 17	NC_000017.10:g.60424045_60424046del
GRCh37.p13 chr 17	NC_000017.10:g.60424046del
GRCh37.p13 chr 17	NC_000017.10:g.60424046dup
GRCh37.p13 chr 17	NC_000017.10:g.60424045_60424046dup
GRCh37.p13 chr 17	NC_000017.10:g.60424044_60424046dup
GRCh37.p13 chr 17	NC_000017.10:g.60424042_60424046dup

Gene: LOC105371936, uncharacterized LOC105371936 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105371936 transcript	XR_934899.1: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)₁₂=	delTT	delT	dupT	dupTT	dupTTT	dup(T)₅
GRCh38.p14 chr 17	NC_000017.11:g.62346674_62346685=	NC_000017.11:g.62346684_62346685del	NC_000017.11:g.62346685del	NC_000017.11:g.62346685dup	NC_000017.11:g.62346684_62346685dup	NC_000017.11:g.62346683_62346685dup	NC_000017.11:g.62346681_62346685dup
GRCh37.p13 chr 17	NC_000017.10:g.60424035_60424046=	NC_000017.10:g.60424045_60424046del	NC_000017.10:g.60424046del	NC_000017.10:g.60424046dup	NC_000017.10:g.60424045_60424046dup	NC_000017.10:g.60424044_60424046dup	NC_000017.10:g.60424042_60424046dup

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#.

58 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40807820	Dec 03, 2013 (138)
2	HUMANGENOME_JCVI	ss95698223	Dec 05, 2013 (138)
3	GMI	ss289333188	May 04, 2012 (137)
4	PJP	ss294919519	May 09, 2011 (137)
5	SSMP	ss664368552	Apr 01, 2015 (144)
6	BILGI_BIOE	ss666696298	Jan 10, 2018 (151)
7	1000GENOMES	ss1376807431	Jan 10, 2018 (151)
8	1000GENOMES	ss1376807432	Aug 21, 2014 (142)
9	DDI	ss1536852277	Jan 10, 2018 (151)
10	EVA_UK10K_ALSPAC	ss1708811585	Jan 10, 2018 (151)
11	EVA_UK10K_TWINSUK	ss1708811774	Jan 10, 2018 (151)
12	EVA_UK10K_TWINSUK	ss1710738533	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1710738550	Apr 01, 2015 (144)
14	HAMMER_LAB	ss1808838700	Jan 10, 2018 (151)
15	SWEGEN	ss3015753227	Jan 10, 2018 (151)
16	URBANLAB	ss3650682207	Oct 12, 2018 (152)
17	EVA_DECODE	ss3700729249	Jul 13, 2019 (153)
18	EVA_DECODE	ss3700729250	Jul 13, 2019 (153)
19	EVA_DECODE	ss3700729251	Jul 13, 2019 (153)
20	EVA_DECODE	ss3700729252	Jul 13, 2019 (153)
21	EVA_DECODE	ss3700729253	Jul 13, 2019 (153)
22	ACPOP	ss3742137116	Jul 13, 2019 (153)
23	ACPOP	ss3742137117	Jul 13, 2019 (153)
24	PACBIO	ss3788241857	Jul 13, 2019 (153)
25	PACBIO	ss3793191800	Jul 13, 2019 (153)
26	PACBIO	ss3798077610	Jul 13, 2019 (153)
27	KHV_HUMAN_GENOMES	ss3820086737	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3820086738	Jul 13, 2019 (153)
29	EVA	ss3834931842	Apr 27, 2020 (154)
30	EVA	ss3846575545	Apr 27, 2020 (154)
31	KOGIC	ss3979105177	Apr 27, 2020 (154)
32	KOGIC	ss3979105178	Apr 27, 2020 (154)
33	KOGIC	ss3979105179	Apr 27, 2020 (154)
34	KOGIC	ss3979105180	Apr 27, 2020 (154)
35	GNOMAD	ss4313988593	Apr 27, 2021 (155)
36	GNOMAD	ss4313988594	Apr 27, 2021 (155)
37	GNOMAD	ss4313988595	Apr 27, 2021 (155)
38	GNOMAD	ss4313988596	Apr 27, 2021 (155)
39	GNOMAD	ss4313988597	Apr 27, 2021 (155)
40	TOMMO_GENOMICS	ss5223048101	Apr 27, 2021 (155)
41	TOMMO_GENOMICS	ss5223048102	Apr 27, 2021 (155)
42	TOMMO_GENOMICS	ss5223048103	Apr 27, 2021 (155)
43	TOMMO_GENOMICS	ss5223048104	Apr 27, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5303602581	Oct 16, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5303602582	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5303602583	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5303602584	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5303602585	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5496599388	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5496599389	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5496599390	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5496599391	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5779454537	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5779454538	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5779454539	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5779454541	Oct 16, 2022 (156)
57	EVA	ss5834161718	Oct 16, 2022 (156)
58	EVA	ss5834161719	Oct 16, 2022 (156)
59	1000Genomes	NC_000017.10 - 60424035	Oct 12, 2018 (152)
60	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 40141386 (NC_000017.10:60424034::T 1558/3854) Row 40141387 (NC_000017.10:60424034:TT: 579/3854)	-	Oct 12, 2018 (152)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 40141386 (NC_000017.10:60424034::T 1558/3854) Row 40141387 (NC_000017.10:60424034:TT: 579/3854)	-	Oct 12, 2018 (152)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511193060 (NC_000017.11:62346673::T 49658/135968) Row 511193061 (NC_000017.11:62346673::TT 3515/136062) Row 511193062 (NC_000017.11:62346673::TTT 37/136106)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511193060 (NC_000017.11:62346673::T 49658/135968) Row 511193061 (NC_000017.11:62346673::TT 3515/136062) Row 511193062 (NC_000017.11:62346673::TTT 37/136106)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511193060 (NC_000017.11:62346673::T 49658/135968) Row 511193061 (NC_000017.11:62346673::TT 3515/136062) Row 511193062 (NC_000017.11:62346673::TTT 37/136106)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511193060 (NC_000017.11:62346673::T 49658/135968) Row 511193061 (NC_000017.11:62346673::TT 3515/136062) Row 511193062 (NC_000017.11:62346673::TTT 37/136106)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511193060 (NC_000017.11:62346673::T 49658/135968) Row 511193061 (NC_000017.11:62346673::TT 3515/136062) Row 511193062 (NC_000017.11:62346673::TTT 37/136106)...	-	Apr 27, 2021 (155)
67	Korean Genome Project Submission ignored due to conflicting rows: Row 35483178 (NC_000017.11:62346675::T 885/1832) Row 35483179 (NC_000017.11:62346674:T: 18/1832) Row 35483180 (NC_000017.11:62346673:TT: 22/1832)...	-	Apr 27, 2020 (154)
68	Korean Genome Project Submission ignored due to conflicting rows: Row 35483178 (NC_000017.11:62346675::T 885/1832) Row 35483179 (NC_000017.11:62346674:T: 18/1832) Row 35483180 (NC_000017.11:62346673:TT: 22/1832)...	-	Apr 27, 2020 (154)
69	Korean Genome Project Submission ignored due to conflicting rows: Row 35483178 (NC_000017.11:62346675::T 885/1832) Row 35483179 (NC_000017.11:62346674:T: 18/1832) Row 35483180 (NC_000017.11:62346673:TT: 22/1832)...	-	Apr 27, 2020 (154)
70	Korean Genome Project Submission ignored due to conflicting rows: Row 35483178 (NC_000017.11:62346675::T 885/1832) Row 35483179 (NC_000017.11:62346674:T: 18/1832) Row 35483180 (NC_000017.11:62346673:TT: 22/1832)...	-	Apr 27, 2020 (154)
71	Northern Sweden Submission ignored due to conflicting rows: Row 15421981 (NC_000017.10:60424034:TT: 81/600) Row 15421982 (NC_000017.10:60424034::T 206/600)	-	Jul 13, 2019 (153)
72	Northern Sweden Submission ignored due to conflicting rows: Row 15421981 (NC_000017.10:60424034:TT: 81/600) Row 15421982 (NC_000017.10:60424034::T 206/600)	-	Jul 13, 2019 (153)
73	8.3KJPN Submission ignored due to conflicting rows: Row 81017408 (NC_000017.10:60424034::T 9230/16760) Row 81017409 (NC_000017.10:60424034:TT: 142/16760) Row 81017410 (NC_000017.10:60424034::TT 66/16760)...	-	Apr 27, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 81017408 (NC_000017.10:60424034::T 9230/16760) Row 81017409 (NC_000017.10:60424034:TT: 142/16760) Row 81017410 (NC_000017.10:60424034::TT 66/16760)...	-	Apr 27, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 81017408 (NC_000017.10:60424034::T 9230/16760) Row 81017409 (NC_000017.10:60424034:TT: 142/16760) Row 81017410 (NC_000017.10:60424034::TT 66/16760)...	-	Apr 27, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 81017408 (NC_000017.10:60424034::T 9230/16760) Row 81017409 (NC_000017.10:60424034:TT: 142/16760) Row 81017410 (NC_000017.10:60424034::TT 66/16760)...	-	Apr 27, 2021 (155)
77	14KJPN Submission ignored due to conflicting rows: Row 113291641 (NC_000017.11:62346673::T 15577/28258) Row 113291642 (NC_000017.11:62346673:T: 21/28258) Row 113291643 (NC_000017.11:62346673:TT: 211/28258)...	-	Oct 16, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 113291641 (NC_000017.11:62346673::T 15577/28258) Row 113291642 (NC_000017.11:62346673:T: 21/28258) Row 113291643 (NC_000017.11:62346673:TT: 211/28258)...	-	Oct 16, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 113291641 (NC_000017.11:62346673::T 15577/28258) Row 113291642 (NC_000017.11:62346673:T: 21/28258) Row 113291643 (NC_000017.11:62346673:TT: 211/28258)...	-	Oct 16, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 113291641 (NC_000017.11:62346673::T 15577/28258) Row 113291642 (NC_000017.11:62346673:T: 21/28258) Row 113291643 (NC_000017.11:62346673:TT: 211/28258)...	-	Oct 16, 2022 (156)
81	UK 10K study - Twins Submission ignored due to conflicting rows: Row 40141386 (NC_000017.10:60424034::T 1460/3708) Row 40141387 (NC_000017.10:60424034:TT: 523/3708)	-	Oct 12, 2018 (152)
82	UK 10K study - Twins Submission ignored due to conflicting rows: Row 40141386 (NC_000017.10:60424034::T 1460/3708) Row 40141387 (NC_000017.10:60424034:TT: 523/3708)	-	Oct 12, 2018 (152)
83	ALFA	NC_000017.11 - 62346674	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)
rs144538005	May 11, 2012 (137)
rs375569286	May 13, 2013 (138)
rs563205084	Apr 01, 2015 (144)
rs796694766	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
72439050, ss666696298, ss1376807431, ss1536852277, ss1708811585, ss1708811774, ss1808838700, ss3015753227, ss3742137116, ss3834931842, ss5223048102, ss5834161718	NC_000017.10:60424034:TT:	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss3700729249, ss3820086738, ss3979105179, ss4313988597, ss5303602581, ss5496599389, ss5779454539	NC_000017.11:62346673:TT:	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTT	(self)
3242039224	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTT	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss5223048104	NC_000017.10:60424034:T:	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4313988596, ss5303602584, ss5496599391, ss5779454538	NC_000017.11:62346673:T:	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
3242039224	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTT	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3700729250, ss3979105178	NC_000017.11:62346674:T:	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss294919519	NC_000017.9:57777770::T	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss289333188	NC_000017.9:57777775::T	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss664368552, ss3742137117, ss3788241857, ss3793191800, ss3798077610, ss5223048101, ss5834161719	NC_000017.10:60424034::T	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss1376807432, ss1710738533, ss1710738550	NC_000017.10:60424036::T	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3650682207, ss4313988593, ss5303602582, ss5496599388, ss5779454537	NC_000017.11:62346673::T	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3242039224	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3700729251, ss3820086737, ss3979105177	NC_000017.11:62346675::T	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss40807820, ss95698223	NT_010783.15:25698198::T	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5223048103	NC_000017.10:60424034::TT	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3846575545, ss4313988594, ss5303602583, ss5496599390, ss5779454541	NC_000017.11:62346673::TT	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
3242039224	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3700729252, ss3979105180	NC_000017.11:62346675::TT	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4313988595, ss5303602585	NC_000017.11:62346673::TTT	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3242039224	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3700729253	NC_000017.11:62346675::TTTTT	NC_000017.11:62346673:TTTTTTTTTTTT… NC_000017.11:62346673:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(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 rs35022195

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

rs35022195