Name: rs34116299
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.

rs34116299

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:1020090-1020101 (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
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.000015 (4/264690, TOPMED)
dupT=0.00004 (1/28258, 14KJPN)
dupT=0.00006 (1/16760, 8.3KJPN) (+ 4 more)
delTT=0.00000 (0/14038, ALFA)
delT=0.00000 (0/14038, ALFA)
dupT=0.00000 (0/14038, ALFA)
dupT=0.0028 (18/6404, 1000G_30x)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ABR : 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	HWEP
Total	Global	14038	TTTTTTTTTTTT=1.00000	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	9680	TTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2896	TTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	114	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000	1.0	N/A
African American	Sub	2782	TTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	112	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000	1.0	N/A
East Asian	Sub	86	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	26	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	146	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	610	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	98	TTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	496	TTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000	1.0	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
TopMed	Global	Study-wide	264690	(T)₁₂=0.999985	delTT=0.000015
14KJPN	JAPANESE	Study-wide	28258	- No frequency provided	dupT=0.00004
8.3KJPN	JAPANESE	Study-wide	16760	- No frequency provided	dupT=0.00006
Allele Frequency Aggregator	Total	Global	14038	(T)₁₂=1.00000	delTT=0.00000, delT=0.00000, dupT=0.00000
Allele Frequency Aggregator	European	Sub	9680	(T)₁₂=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000
Allele Frequency Aggregator	African	Sub	2896	(T)₁₂=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	(T)₁₂=1.000	delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Other	Sub	496	(T)₁₂=1.000	delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	(T)₁₂=1.000	delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Asian	Sub	112	(T)₁₂=1.000	delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	South Asian	Sub	98	(T)₁₂=1.00	delTT=0.00, delT=0.00, dupT=0.00
1000Genomes_30x	Global	Study-wide	6404	- No frequency provided	dupT=0.0028
1000Genomes_30x	African	Sub	1786	- No frequency provided	dupT=0.0000
1000Genomes_30x	Europe	Sub	1266	- No frequency provided	dupT=0.0000
1000Genomes_30x	South Asian	Sub	1202	- No frequency provided	dupT=0.0133
1000Genomes_30x	East Asian	Sub	1170	- No frequency provided	dupT=0.0017
1000Genomes_30x	American	Sub	980	- No frequency provided	dupT=0.000

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.1020100_1020101del
GRCh38.p14 chr 17	NC_000017.11:g.1020101del
GRCh38.p14 chr 17	NC_000017.11:g.1020101dup
GRCh37.p13 chr 17	NC_000017.10:g.923340_923341del
GRCh37.p13 chr 17	NC_000017.10:g.923341del
GRCh37.p13 chr 17	NC_000017.10:g.923341dup
ABR RefSeqGene	NG_011987.2:g.214590_214591del
ABR RefSeqGene	NG_011987.2:g.214591del
ABR RefSeqGene	NG_011987.2:g.214591dup
GRCh38.p14 chr 17 alt locus HSCHR17_2_CTG2	NT_187613.1:g.59347_59348del
GRCh38.p14 chr 17 alt locus HSCHR17_2_CTG2	NT_187613.1:g.59348del
GRCh38.p14 chr 17 alt locus HSCHR17_2_CTG2	NT_187613.1:g.59348dup
GRCh38.p14 chr 17 alt locus HSCHR17_3_CTG2	NT_187664.1:g.59347_59348del
GRCh38.p14 chr 17 alt locus HSCHR17_3_CTG2	NT_187664.1:g.59348del
GRCh38.p14 chr 17 alt locus HSCHR17_3_CTG2	NT_187664.1:g.59348dup

Gene: ABR, ABR activator of RhoGEF and GTPase (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ABR transcript variant 2	NM_001092.5:c.1681-6927_1… NM_001092.5:c.1681-6927_1681-6926del	N/A	Intron Variant
ABR transcript variant 3	NM_001159746.3:c.1654-692… NM_001159746.3:c.1654-6927_1654-6926del	N/A	Intron Variant
ABR transcript variant 4	NM_001256847.3:c.145-6927… NM_001256847.3:c.145-6927_145-6926del	N/A	Intron Variant
ABR transcript variant 5	NM_001282149.2:c.1138-692… NM_001282149.2:c.1138-6927_1138-6926del	N/A	Intron Variant
ABR transcript variant 6	NM_001322840.2:c.1654-692… NM_001322840.2:c.1654-6927_1654-6926del	N/A	Intron Variant
ABR transcript variant 7	NM_001322841.2:c.2569-692… NM_001322841.2:c.2569-6927_2569-6926del	N/A	Intron Variant
ABR transcript variant 1	NM_021962.5:c.1792-6927_1… NM_021962.5:c.1792-6927_1792-6926del	N/A	Intron Variant
ABR transcript variant 8	NM_001322842.2:c.	N/A	Genic Downstream Transcript Variant
ABR transcript variant X7	XM_011523810.4:c.1792-692… XM_011523810.4:c.1792-6927_1792-6926del	N/A	Intron Variant
ABR transcript variant X10	XM_011523812.4:c.1753-692… XM_011523812.4:c.1753-6927_1753-6926del	N/A	Intron Variant
ABR transcript variant X11	XM_011523813.4:c.1681-692… XM_011523813.4:c.1681-6927_1681-6926del	N/A	Intron Variant
ABR transcript variant X12	XM_011523814.4:c.1654-692… XM_011523814.4:c.1654-6927_1654-6926del	N/A	Intron Variant
ABR transcript variant X13	XM_011523815.4:c.1654-692… XM_011523815.4:c.1654-6927_1654-6926del	N/A	Intron Variant
ABR transcript variant X1	XM_017024539.2:c.2569-692… XM_017024539.2:c.2569-6927_2569-6926del	N/A	Intron Variant
ABR transcript variant X2	XM_017024540.3:c.2470-692… XM_017024540.3:c.2470-6927_2470-6926del	N/A	Intron Variant
ABR transcript variant X16	XM_017024542.3:c.1147-692… XM_017024542.3:c.1147-6927_1147-6926del	N/A	Intron Variant
ABR transcript variant X17	XM_017024543.3:c.1138-692… XM_017024543.3:c.1138-6927_1138-6926del	N/A	Intron Variant
ABR transcript variant X3	XM_047435860.1:c.2470-692… XM_047435860.1:c.2470-6927_2470-6926del	N/A	Intron Variant
ABR transcript variant X4	XM_047435861.1:c.2569-692… XM_047435861.1:c.2569-6927_2569-6926del	N/A	Intron Variant
ABR transcript variant X5	XM_047435862.1:c.2569-692… XM_047435862.1:c.2569-6927_2569-6926del	N/A	Intron Variant
ABR transcript variant X8	XM_047435863.1:c.1789-692… XM_047435863.1:c.1789-6927_1789-6926del	N/A	Intron Variant
ABR transcript variant X14	XM_047435864.1:c.1654-692… XM_047435864.1:c.1654-6927_1654-6926del	N/A	Intron Variant
ABR transcript variant X15	XM_047435865.1:c.1522-692… XM_047435865.1:c.1522-6927_1522-6926del	N/A	Intron Variant
ABR transcript variant X9	XM_011523811.4:c.	N/A	Genic Downstream Transcript Variant
ABR transcript variant X6	XR_007065294.1: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
GRCh38.p14 chr 17	NC_000017.11:g.1020090_1020101=	NC_000017.11:g.1020100_1020101del	NC_000017.11:g.1020101del	NC_000017.11:g.1020101dup
GRCh37.p13 chr 17	NC_000017.10:g.923330_923341=	NC_000017.10:g.923340_923341del	NC_000017.10:g.923341del	NC_000017.10:g.923341dup
ABR RefSeqGene	NG_011987.2:g.214580_214591=	NG_011987.2:g.214590_214591del	NG_011987.2:g.214591del	NG_011987.2:g.214591dup
GRCh38.p14 chr 17 alt locus HSCHR17_2_CTG2	NT_187613.1:g.59337_59348=	NT_187613.1:g.59347_59348del	NT_187613.1:g.59348del	NT_187613.1:g.59348dup
GRCh38.p14 chr 17 alt locus HSCHR17_3_CTG2	NT_187664.1:g.59337_59348=	NT_187664.1:g.59347_59348del	NT_187664.1:g.59348del	NT_187664.1:g.59348dup
ABR transcript variant 2	NM_001092.4:c.1681-6926=	NM_001092.4:c.1681-6927_1681-6926del	NM_001092.4:c.1681-6926del	NM_001092.4:c.1681-6926dup
ABR transcript variant 2	NM_001092.5:c.1681-6926=	NM_001092.5:c.1681-6927_1681-6926del	NM_001092.5:c.1681-6926del	NM_001092.5:c.1681-6926dup
ABR transcript variant 3	NM_001159746.2:c.1654-6926=	NM_001159746.2:c.1654-6927_1654-6926del	NM_001159746.2:c.1654-6926del	NM_001159746.2:c.1654-6926dup
ABR transcript variant 3	NM_001159746.3:c.1654-6926=	NM_001159746.3:c.1654-6927_1654-6926del	NM_001159746.3:c.1654-6926del	NM_001159746.3:c.1654-6926dup
ABR transcript variant 4	NM_001256847.1:c.145-6926=	NM_001256847.1:c.145-6927_145-6926del	NM_001256847.1:c.145-6926del	NM_001256847.1:c.145-6926dup
ABR transcript variant 4	NM_001256847.3:c.145-6926=	NM_001256847.3:c.145-6927_145-6926del	NM_001256847.3:c.145-6926del	NM_001256847.3:c.145-6926dup
ABR transcript variant 5	NM_001282149.2:c.1138-6926=	NM_001282149.2:c.1138-6927_1138-6926del	NM_001282149.2:c.1138-6926del	NM_001282149.2:c.1138-6926dup
ABR transcript variant 6	NM_001322840.2:c.1654-6926=	NM_001322840.2:c.1654-6927_1654-6926del	NM_001322840.2:c.1654-6926del	NM_001322840.2:c.1654-6926dup
ABR transcript variant 7	NM_001322841.2:c.2569-6926=	NM_001322841.2:c.2569-6927_2569-6926del	NM_001322841.2:c.2569-6926del	NM_001322841.2:c.2569-6926dup
ABR transcript variant 1	NM_021962.3:c.1792-6926=	NM_021962.3:c.1792-6927_1792-6926del	NM_021962.3:c.1792-6926del	NM_021962.3:c.1792-6926dup
ABR transcript variant 1	NM_021962.5:c.1792-6926=	NM_021962.5:c.1792-6927_1792-6926del	NM_021962.5:c.1792-6926del	NM_021962.5:c.1792-6926dup
ABR transcript variant X7	XM_011523810.4:c.1792-6926=	XM_011523810.4:c.1792-6927_1792-6926del	XM_011523810.4:c.1792-6926del	XM_011523810.4:c.1792-6926dup
ABR transcript variant X10	XM_011523812.4:c.1753-6926=	XM_011523812.4:c.1753-6927_1753-6926del	XM_011523812.4:c.1753-6926del	XM_011523812.4:c.1753-6926dup
ABR transcript variant X11	XM_011523813.4:c.1681-6926=	XM_011523813.4:c.1681-6927_1681-6926del	XM_011523813.4:c.1681-6926del	XM_011523813.4:c.1681-6926dup
ABR transcript variant X12	XM_011523814.4:c.1654-6926=	XM_011523814.4:c.1654-6927_1654-6926del	XM_011523814.4:c.1654-6926del	XM_011523814.4:c.1654-6926dup
ABR transcript variant X13	XM_011523815.4:c.1654-6926=	XM_011523815.4:c.1654-6927_1654-6926del	XM_011523815.4:c.1654-6926del	XM_011523815.4:c.1654-6926dup
ABR transcript variant X1	XM_017024539.2:c.2569-6926=	XM_017024539.2:c.2569-6927_2569-6926del	XM_017024539.2:c.2569-6926del	XM_017024539.2:c.2569-6926dup
ABR transcript variant X2	XM_017024540.3:c.2470-6926=	XM_017024540.3:c.2470-6927_2470-6926del	XM_017024540.3:c.2470-6926del	XM_017024540.3:c.2470-6926dup
ABR transcript variant X16	XM_017024542.3:c.1147-6926=	XM_017024542.3:c.1147-6927_1147-6926del	XM_017024542.3:c.1147-6926del	XM_017024542.3:c.1147-6926dup
ABR transcript variant X17	XM_017024543.3:c.1138-6926=	XM_017024543.3:c.1138-6927_1138-6926del	XM_017024543.3:c.1138-6926del	XM_017024543.3:c.1138-6926dup
ABR transcript variant X3	XM_047435860.1:c.2470-6926=	XM_047435860.1:c.2470-6927_2470-6926del	XM_047435860.1:c.2470-6926del	XM_047435860.1:c.2470-6926dup
ABR transcript variant X4	XM_047435861.1:c.2569-6926=	XM_047435861.1:c.2569-6927_2569-6926del	XM_047435861.1:c.2569-6926del	XM_047435861.1:c.2569-6926dup
ABR transcript variant X5	XM_047435862.1:c.2569-6926=	XM_047435862.1:c.2569-6927_2569-6926del	XM_047435862.1:c.2569-6926del	XM_047435862.1:c.2569-6926dup
ABR transcript variant X8	XM_047435863.1:c.1789-6926=	XM_047435863.1:c.1789-6927_1789-6926del	XM_047435863.1:c.1789-6926del	XM_047435863.1:c.1789-6926dup
ABR transcript variant X14	XM_047435864.1:c.1654-6926=	XM_047435864.1:c.1654-6927_1654-6926del	XM_047435864.1:c.1654-6926del	XM_047435864.1:c.1654-6926dup
ABR transcript variant X15	XM_047435865.1:c.1522-6926=	XM_047435865.1:c.1522-6927_1522-6926del	XM_047435865.1:c.1522-6926del	XM_047435865.1:c.1522-6926dup

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#.

12 SubSNP, 8 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40851933	Mar 13, 2006 (126)
2	SSIP	ss947362876	Aug 21, 2014 (142)
3	PACBIO	ss3788126757	Jul 13, 2019 (153)
4	GNOMAD	ss4306662427	Apr 27, 2021 (155)
5	GNOMAD	ss4306662428	Apr 27, 2021 (155)
6	GNOMAD	ss4306662429	Apr 27, 2021 (155)
7	TOPMED	ss5026910434	Apr 27, 2021 (155)
8	TOMMO_GENOMICS	ss5221122122	Apr 27, 2021 (155)
9	1000G_HIGH_COVERAGE	ss5302145337	Oct 17, 2022 (156)
10	1000G_HIGH_COVERAGE	ss5605380188	Oct 17, 2022 (156)
11	TOMMO_GENOMICS	ss5776599189	Oct 17, 2022 (156)
12	YY_MCH	ss5816264678	Oct 17, 2022 (156)
13	1000Genomes_30x	NC_000017.11 - 1020090	Oct 17, 2022 (156)
14	gnomAD - Genomes Submission ignored due to conflicting rows: Row 499277748 (NC_000017.11:1020089::T 31/137482) Row 499277749 (NC_000017.11:1020089:T: 96/137312) Row 499277750 (NC_000017.11:1020089:TT: 1/137514)	-	Apr 27, 2021 (155)
15	gnomAD - Genomes Submission ignored due to conflicting rows: Row 499277748 (NC_000017.11:1020089::T 31/137482) Row 499277749 (NC_000017.11:1020089:T: 96/137312) Row 499277750 (NC_000017.11:1020089:TT: 1/137514)	-	Apr 27, 2021 (155)
16	gnomAD - Genomes Submission ignored due to conflicting rows: Row 499277748 (NC_000017.11:1020089::T 31/137482) Row 499277749 (NC_000017.11:1020089:T: 96/137312) Row 499277750 (NC_000017.11:1020089:TT: 1/137514)	-	Apr 27, 2021 (155)
17	8.3KJPN	NC_000017.10 - 923330	Apr 27, 2021 (155)
18	14KJPN	NC_000017.11 - 1020090	Oct 17, 2022 (156)
19	TopMed	NC_000017.11 - 1020090	Apr 27, 2021 (155)
20	ALFA	NC_000017.11 - 1020090	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
242456096, ss4306662429, ss5026910434	NC_000017.11:1020089:TT:	NC_000017.11:1020089:TTTTTTTTTTTT:… NC_000017.11:1020089:TTTTTTTTTTTT:TTTTTTTTTT	(self)
8594841941	NC_000017.11:1020089:TTTTTTTTTTTT:… NC_000017.11:1020089:TTTTTTTTTTTT:TTTTTTTTTT	NC_000017.11:1020089:TTTTTTTTTTTT:… NC_000017.11:1020089:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss3788126757	NC_000017.10:923329:T:	NC_000017.11:1020089:TTTTTTTTTTTT:… NC_000017.11:1020089:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4306662428, ss5816264678	NC_000017.11:1020089:T:	NC_000017.11:1020089:TTTTTTTTTTTT:… NC_000017.11:1020089:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
8594841941	NC_000017.11:1020089:TTTTTTTTTTTT:… NC_000017.11:1020089:TTTTTTTTTTTT:TTTTTTTTTTT	NC_000017.11:1020089:TTTTTTTTTTTT:… NC_000017.11:1020089:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
79091429, ss947362876, ss5221122122	NC_000017.10:923329::T	NC_000017.11:1020089:TTTTTTTTTTTT:… NC_000017.11:1020089:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
92906123, 110436293, ss4306662427, ss5302145337, ss5605380188, ss5776599189	NC_000017.11:1020089::T	NC_000017.11:1020089:TTTTTTTTTTTT:… NC_000017.11:1020089:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
8594841941	NC_000017.11:1020089:TTTTTTTTTTTT:… NC_000017.11:1020089:TTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000017.11:1020089:TTTTTTTTTTTT:… NC_000017.11:1020089:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss40851933	NT_010718.16:526715::T	NC_000017.11:1020089:TTTTTTTTTTTT:… NC_000017.11:1020089:TTTTTTTTTTTT:TTTTTTTTTTTTT	(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 rs34116299

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

rs34116299