Name: rs34120446
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.

rs34120446

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:182716475-182716484 (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
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.016000 (4235/264690, TOPMED)
delT=0.01948 (261/13400, ALFA)
delTT=0.0225 (103/4576, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RGS8 : 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	13400	TTTTTTTTTT=0.96448	TTTTTTTT=0.00000, TTTTTTTTT=0.01948, TTTTTTTTTTT=0.01604, TTTTTTTTTTTT=0.00000	0.962131	0.001539	0.03633	13
European	Sub	9980	TTTTTTTTTT=0.9524	TTTTTTTT=0.0000, TTTTTTTTT=0.0261, TTTTTTTTTTT=0.0215, TTTTTTTTTTTT=0.0000	0.948809	0.002089	0.049102	8
African	Sub	2236	TTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	90	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	2146	TTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	92	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	72	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	20	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	114	TTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	520	TTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	78	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	380	TTTTTTTTTT=0.997	TTTTTTTT=0.000, TTTTTTTTT=0.003, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000	0.994737	0.0	0.005263	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
TopMed	Global	Study-wide	264690	(T)₁₀=0.984000	delTT=0.016000
Allele Frequency Aggregator	Total	Global	13400	(T)₁₀=0.96448	delTT=0.00000, delT=0.01948, dupT=0.01604, dupTT=0.00000
Allele Frequency Aggregator	European	Sub	9980	(T)₁₀=0.9524	delTT=0.0000, delT=0.0261, dupT=0.0215, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	2236	(T)₁₀=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	520	(T)₁₀=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	380	(T)₁₀=0.997	delTT=0.000, delT=0.003, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	114	(T)₁₀=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Asian	Sub	92	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	78	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	4576	(T)₁₀=0.9775	delTT=0.0225
1000Genomes	African	Sub	1242	(T)₁₀=0.9211	delTT=0.0789
1000Genomes	East Asian	Sub	953	(T)₁₀=0.999	delTT=0.001
1000Genomes	Europe	Sub	876	(T)₁₀=1.000	delTT=0.000
1000Genomes	South Asian	Sub	858	(T)₁₀=1.000	delTT=0.000
1000Genomes	American	Sub	647	(T)₁₀=0.994	delTT=0.006

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 1	NC_000001.11:g.182716483_182716484del
GRCh38.p14 chr 1	NC_000001.11:g.182716484del
GRCh38.p14 chr 1	NC_000001.11:g.182716484dup
GRCh38.p14 chr 1	NC_000001.11:g.182716483_182716484dup
GRCh37.p13 chr 1	NC_000001.10:g.182685618_182685619del
GRCh37.p13 chr 1	NC_000001.10:g.182685619del
GRCh37.p13 chr 1	NC_000001.10:g.182685619dup
GRCh37.p13 chr 1	NC_000001.10:g.182685618_182685619dup

Gene: RGS8, regulator of G protein signaling 8 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RGS8 transcript variant 4	NM_001387847.1:c.-292+357… NM_001387847.1:c.-292+35776_-292+35777del	N/A	Intron Variant
RGS8 transcript variant 2	NM_001102450.3:c.	N/A	Genic Upstream Transcript Variant
RGS8 transcript variant 3	NM_001369564.2:c.	N/A	Genic Upstream Transcript Variant
RGS8 transcript variant 5	NM_001387848.1:c.	N/A	Genic Upstream Transcript Variant
RGS8 transcript variant 6	NM_001387849.1:c.	N/A	Genic Upstream Transcript Variant
RGS8 transcript variant 1	NM_033345.4:c.	N/A	Genic Upstream Transcript Variant
RGS8 transcript variant X2	XM_011510089.4:c.-109+357… XM_011510089.4:c.-109+35776_-109+35777del	N/A	Intron Variant
RGS8 transcript variant X1	XM_017002631.3:c.	N/A	Genic Upstream Transcript Variant
RGS8 transcript variant X3	XM_047432939.1:c.	N/A	Genic 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)₁₀=	delTT	delT	dupT	dupTT
GRCh38.p14 chr 1	NC_000001.11:g.182716475_182716484=	NC_000001.11:g.182716483_182716484del	NC_000001.11:g.182716484del	NC_000001.11:g.182716484dup	NC_000001.11:g.182716483_182716484dup
GRCh37.p13 chr 1	NC_000001.10:g.182685610_182685619=	NC_000001.10:g.182685618_182685619del	NC_000001.10:g.182685619del	NC_000001.10:g.182685619dup	NC_000001.10:g.182685618_182685619dup
RGS8 transcript variant 4	NM_001387847.1:c.-292+35777=	NM_001387847.1:c.-292+35776_-292+35777del	NM_001387847.1:c.-292+35777del	NM_001387847.1:c.-292+35777dup	NM_001387847.1:c.-292+35776_-292+35777dup
RGS8 transcript variant X2	XM_011510089.4:c.-109+35777=	XM_011510089.4:c.-109+35776_-109+35777del	XM_011510089.4:c.-109+35777del	XM_011510089.4:c.-109+35777dup	XM_011510089.4:c.-109+35776_-109+35777dup

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#.

46 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41257478	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss98579108	Feb 13, 2009 (137)
3	GMI	ss288063182	May 04, 2012 (137)
4	LUNTER	ss550999192	Apr 25, 2013 (138)
5	LUNTER	ss551022109	Jan 10, 2018 (151)
6	TISHKOFF	ss553794532	Jan 10, 2018 (151)
7	TISHKOFF	ss553794534	Apr 25, 2013 (138)
8	SSMP	ss663137640	Apr 01, 2015 (144)
9	BILGI_BIOE	ss666118441	Apr 25, 2013 (138)
10	1000GENOMES	ss1367917955	Jan 10, 2018 (151)
11	1000GENOMES	ss1367917956	Aug 21, 2014 (142)
12	1000GENOMES	ss1367917957	Aug 21, 2014 (144)
13	EVA_UK10K_ALSPAC	ss1701493272	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1701493275	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1709960054	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1709960069	Apr 01, 2015 (144)
17	HAMMER_LAB	ss1795373952	Sep 08, 2015 (146)
18	SWEGEN	ss2988064661	Nov 08, 2017 (151)
19	BIOINF_KMB_FNS_UNIBA	ss3645083896	Oct 11, 2018 (152)
20	URBANLAB	ss3646833771	Oct 11, 2018 (152)
21	EVA_DECODE	ss3688161590	Jul 12, 2019 (153)
22	EVA_DECODE	ss3688161591	Jul 12, 2019 (153)
23	ACPOP	ss3727654579	Jul 12, 2019 (153)
24	ACPOP	ss3727654580	Jul 12, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3800046972	Jul 12, 2019 (153)
26	KHV_HUMAN_GENOMES	ss3800046973	Jul 12, 2019 (153)
27	EVA	ss3826525223	Apr 25, 2020 (154)
28	GNOMAD	ss4007090481	Apr 25, 2021 (155)
29	GNOMAD	ss4007090482	Apr 25, 2021 (155)
30	GNOMAD	ss4007090483	Apr 25, 2021 (155)
31	TOPMED	ss4475164169	Apr 25, 2021 (155)
32	TOMMO_GENOMICS	ss5147358731	Apr 25, 2021 (155)
33	TOMMO_GENOMICS	ss5147358732	Apr 25, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5244966448	Oct 12, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5244966449	Oct 12, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5244966450	Oct 12, 2022 (156)
37	HUGCELL_USP	ss5445484731	Oct 12, 2022 (156)
38	HUGCELL_USP	ss5445484732	Oct 12, 2022 (156)
39	HUGCELL_USP	ss5445484733	Oct 12, 2022 (156)
40	TOMMO_GENOMICS	ss5674810708	Oct 12, 2022 (156)
41	TOMMO_GENOMICS	ss5674810709	Oct 12, 2022 (156)
42	YY_MCH	ss5801427738	Oct 12, 2022 (156)
43	EVA	ss5832932433	Oct 12, 2022 (156)
44	EVA	ss5832932434	Oct 12, 2022 (156)
45	EVA	ss5849185599	Oct 12, 2022 (156)
46	EVA	ss5911023230	Oct 12, 2022 (156)
47	1000Genomes	NC_000001.10 - 182685610	Oct 11, 2018 (152)
48	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 2479682 (NC_000001.10:182685609::T 272/3854) Row 2479683 (NC_000001.10:182685609:T: 279/3854)	-	Oct 11, 2018 (152)
49	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 2479682 (NC_000001.10:182685609::T 272/3854) Row 2479683 (NC_000001.10:182685609:T: 279/3854)	-	Oct 11, 2018 (152)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32656964 (NC_000001.11:182716474::T 7543/135762) Row 32656965 (NC_000001.11:182716474::TT 4/135934) Row 32656966 (NC_000001.11:182716474:T: 7247/135918)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32656964 (NC_000001.11:182716474::T 7543/135762) Row 32656965 (NC_000001.11:182716474::TT 4/135934) Row 32656966 (NC_000001.11:182716474:T: 7247/135918)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32656964 (NC_000001.11:182716474::T 7543/135762) Row 32656965 (NC_000001.11:182716474::TT 4/135934) Row 32656966 (NC_000001.11:182716474:T: 7247/135918)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 32656964 (NC_000001.11:182716474::T 7543/135762) Row 32656965 (NC_000001.11:182716474::TT 4/135934) Row 32656966 (NC_000001.11:182716474:T: 7247/135918)...	-	Apr 25, 2021 (155)
54	Northern Sweden Submission ignored due to conflicting rows: Row 939444 (NC_000001.10:182685609::T 56/600) Row 939445 (NC_000001.10:182685609:T: 36/600)	-	Jul 12, 2019 (153)
55	Northern Sweden Submission ignored due to conflicting rows: Row 939444 (NC_000001.10:182685609::T 56/600) Row 939445 (NC_000001.10:182685609:T: 36/600)	-	Jul 12, 2019 (153)
56	8.3KJPN Submission ignored due to conflicting rows: Row 5328038 (NC_000001.10:182685609::T 693/16760) Row 5328039 (NC_000001.10:182685609:T: 9/16760)	-	Apr 25, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 5328038 (NC_000001.10:182685609::T 693/16760) Row 5328039 (NC_000001.10:182685609:T: 9/16760)	-	Apr 25, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 8647812 (NC_000001.11:182716474::T 1162/28256) Row 8647813 (NC_000001.11:182716474:T: 20/28256)	-	Oct 12, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 8647812 (NC_000001.11:182716474::T 1162/28256) Row 8647813 (NC_000001.11:182716474:T: 20/28256)	-	Oct 12, 2022 (156)
60	TopMed	NC_000001.11 - 182716475	Apr 25, 2021 (155)
61	UK 10K study - Twins Submission ignored due to conflicting rows: Row 2479682 (NC_000001.10:182685609::T 282/3708) Row 2479683 (NC_000001.10:182685609:T: 265/3708)	-	Oct 11, 2018 (152)
62	UK 10K study - Twins Submission ignored due to conflicting rows: Row 2479682 (NC_000001.10:182685609::T 282/3708) Row 2479683 (NC_000001.10:182685609:T: 265/3708)	-	Oct 11, 2018 (152)
63	ALFA	NC_000001.11 - 182716475	Apr 25, 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)
rs569698460	Apr 01, 2015 (144)
rs796116223	Nov 08, 2017 (151)
rs796940996	Nov 08, 2017 (151)
rs71573282	May 11, 2012 (137)
rs375441172	May 15, 2013 (138)
rs373509735	May 15, 2013 (138)
rs376558488	May 13, 2013 (138)
rs376656614	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss551022109	NC_000001.9:180952232:TT:	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTT	(self)
4524005, ss1367917955	NC_000001.10:182685609:TT:	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTT	(self)
ss553794532	NC_000001.10:182685610:TT:	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTT	(self)
38770504, ss4007090483, ss4475164169, ss5244966450, ss5445484732, ss5911023230	NC_000001.11:182716474:TT:	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTT	(self)
11209479803	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTT	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTT	(self)
ss1701493272, ss1701493275, ss2988064661, ss3727654580, ss3826525223, ss5147358732, ss5832932434	NC_000001.10:182685609:T:	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTT	(self)
ss1367917956	NC_000001.10:182685610:T:	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTT	(self)
ss553794534	NC_000001.10:182685618:T:	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTT	(self)
ss3646833771, ss3688161590, ss5244966448, ss5445484733, ss5674810709	NC_000001.11:182716474:T:	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTT	(self)
11209479803	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTT	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTT	(self)
ss3800046973	NC_000001.11:182716475:T:	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTT	(self)
ss41257478	NT_004487.19:34174251:T:	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTT	(self)
ss98579108	NT_004487.19:34174260:T:	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTT	(self)
ss550999192	NC_000001.9:180952232::T	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss288063182	NC_000001.9:180952242::T	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss663137640, ss666118441, ss1795373952, ss3727654579, ss5147358731, ss5832932433	NC_000001.10:182685609::T	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss1709960054, ss1709960069	NC_000001.10:182685610::T	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss1367917957	NC_000001.10:182685611::T	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3645083896, ss4007090481, ss5244966449, ss5445484731, ss5674810708, ss5801427738, ss5849185599	NC_000001.11:182716474::T	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTTTT	(self)
11209479803	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTTTT	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3688161591	NC_000001.11:182716475::T	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3800046972	NC_000001.11:182716476::T	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss4007090482	NC_000001.11:182716474::TT	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTTTTT	(self)
11209479803	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTTTTT	NC_000001.11:182716474:TTTTTTTTTT:… NC_000001.11:182716474:TTTTTTTTTT:TTTTTTTTTTTT	(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 rs34120446

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
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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

rs34120446