Name: rs9511494
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.

rs9511494

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:24874568 (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: C>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.222018 (58766/264690, TOPMED)
T=0.230300 (32166/139670, GnomAD)
T=0.19690 (5564/28258, 14KJPN) (+ 15 more)
T=0.27364 (5168/18886, ALFA)
T=0.20104 (3369/16758, 8.3KJPN)
T=0.2057 (1317/6404, 1000G_30x)
T=0.2107 (1055/5008, 1000G)
T=0.3742 (1675/4476, Estonian)
T=0.2880 (1110/3854, ALSPAC)
T=0.2778 (1030/3708, TWINSUK)
T=0.2502 (733/2930, KOREAN)
T=0.2598 (476/1832, Korea1K)
T=0.307 (306/998, GoNL)
T=0.332 (199/600, NorthernSweden)
T=0.264 (57/216, Qatari)
T=0.361 (75/208, Vietnamese)
C=0.449 (88/196, SGDP_PRJ)
C=0.42 (10/24, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RNF17 : 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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	18886	C=0.72636	T=0.27364
European	Sub	14282	C=0.68807	T=0.31193
African	Sub	2946	C=0.8758	T=0.1242
African Others	Sub	114	C=0.895	T=0.105
African American	Sub	2832	C=0.8750	T=0.1250
Asian	Sub	112	C=0.777	T=0.223
East Asian	Sub	86	C=0.79	T=0.21
Other Asian	Sub	26	C=0.73	T=0.27
Latin American 1	Sub	146	C=0.795	T=0.205
Latin American 2	Sub	610	C=0.790	T=0.210
South Asian	Sub	98	C=0.86	T=0.14
Other	Sub	692	C=0.783	T=0.217

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	C=0.777982	T=0.222018
gnomAD - Genomes	Global	Study-wide	139670	C=0.769700	T=0.230300
gnomAD - Genomes	European	Sub	75670	C=0.70722	T=0.29278
gnomAD - Genomes	African	Sub	41824	C=0.87930	T=0.12070
gnomAD - Genomes	American	Sub	13594	C=0.79844	T=0.20156
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	C=0.7377	T=0.2623
gnomAD - Genomes	East Asian	Sub	3116	C=0.7214	T=0.2786
gnomAD - Genomes	Other	Sub	2146	C=0.7745	T=0.2255
14KJPN	JAPANESE	Study-wide	28258	C=0.80310	T=0.19690
Allele Frequency Aggregator	Total	Global	18886	C=0.72636	T=0.27364
Allele Frequency Aggregator	European	Sub	14282	C=0.68807	T=0.31193
Allele Frequency Aggregator	African	Sub	2946	C=0.8758	T=0.1242
Allele Frequency Aggregator	Other	Sub	692	C=0.783	T=0.217
Allele Frequency Aggregator	Latin American 2	Sub	610	C=0.790	T=0.210
Allele Frequency Aggregator	Latin American 1	Sub	146	C=0.795	T=0.205
Allele Frequency Aggregator	Asian	Sub	112	C=0.777	T=0.223
Allele Frequency Aggregator	South Asian	Sub	98	C=0.86	T=0.14
8.3KJPN	JAPANESE	Study-wide	16758	C=0.79896	T=0.20104
1000Genomes_30x	Global	Study-wide	6404	C=0.7943	T=0.2057
1000Genomes_30x	African	Sub	1786	C=0.9199	T=0.0801
1000Genomes_30x	Europe	Sub	1266	C=0.7062	T=0.2938
1000Genomes_30x	South Asian	Sub	1202	C=0.8161	T=0.1839
1000Genomes_30x	East Asian	Sub	1170	C=0.6846	T=0.3154
1000Genomes_30x	American	Sub	980	C=0.784	T=0.216
1000Genomes	Global	Study-wide	5008	C=0.7893	T=0.2107
1000Genomes	African	Sub	1322	C=0.9160	T=0.0840
1000Genomes	East Asian	Sub	1008	C=0.6806	T=0.3194
1000Genomes	Europe	Sub	1006	C=0.7097	T=0.2903
1000Genomes	South Asian	Sub	978	C=0.819	T=0.181
1000Genomes	American	Sub	694	C=0.780	T=0.220
Genetic variation in the Estonian population	Estonian	Study-wide	4476	C=0.6258	T=0.3742
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.7120	T=0.2880
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.7222	T=0.2778
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.7498	G=0.0000, T=0.2502
Korean Genome Project	KOREAN	Study-wide	1832	C=0.7402	T=0.2598
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.693	T=0.307
Northern Sweden	ACPOP	Study-wide	600	C=0.668	T=0.332
Qatari	Global	Study-wide	216	C=0.736	T=0.264
A Vietnamese Genetic Variation Database	Global	Study-wide	208	C=0.639	T=0.361
SGDP_PRJ	Global	Study-wide	196	C=0.449	T=0.551
Siberian	Global	Study-wide	24	C=0.42	T=0.58

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 13	NC_000013.11:g.24874568C>G
GRCh38.p14 chr 13	NC_000013.11:g.24874568C>T
GRCh37.p13 chr 13	NC_000013.10:g.25448706C>G
GRCh37.p13 chr 13	NC_000013.10:g.25448706C>T

Gene: RNF17, ring finger protein 17 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RNF17 transcript variant 2	NM_001184993.2:c.4571+319… NM_001184993.2:c.4571+319C>G	N/A	Intron Variant
RNF17 transcript variant 1	NM_031277.3:c.4583+319C>G	N/A	Intron Variant
RNF17 transcript variant X5	XM_006719846.4:c.4790+319… XM_006719846.4:c.4790+319C>G	N/A	Intron Variant
RNF17 transcript variant X6	XM_006719849.3:c.4730+319… XM_006719849.3:c.4730+319C>G	N/A	Intron Variant
RNF17 transcript variant X1	XM_011535152.3:c.4811+319… XM_011535152.3:c.4811+319C>G	N/A	Intron Variant
RNF17 transcript variant X3	XM_011535155.3:c.4811+319… XM_011535155.3:c.4811+319C>G	N/A	Intron Variant
RNF17 transcript variant X2	XM_011535156.3:c.4811+319… XM_011535156.3:c.4811+319C>G	N/A	Intron Variant
RNF17 transcript variant X4	XM_011535157.3:c.4799+319… XM_011535157.3:c.4799+319C>G	N/A	Intron Variant
RNF17 transcript variant X7	XM_011535158.3:c.4685+319… XM_011535158.3:c.4685+319C>G	N/A	Intron Variant
RNF17 transcript variant X8	XM_011535159.3:c.4664+319… XM_011535159.3:c.4664+319C>G	N/A	Intron Variant
RNF17 transcript variant X9	XM_011535160.3:c.4652+319… XM_011535160.3:c.4652+319C>G	N/A	Intron Variant
RNF17 transcript variant X12	XM_011535162.2:c.4208+319… XM_011535162.2:c.4208+319C>G	N/A	Intron Variant
RNF17 transcript variant X13	XM_011535163.2:c.3497+319… XM_011535163.2:c.3497+319C>G	N/A	Intron Variant
RNF17 transcript variant X14	XM_011535164.3:c.2381+319… XM_011535164.3:c.2381+319C>G	N/A	Intron Variant
RNF17 transcript variant X10	XM_017020676.2:c.4547+319… XM_017020676.2:c.4547+319C>G	N/A	Intron Variant
RNF17 transcript variant X15	XM_047430486.1:c.4811+319… XM_047430486.1:c.4811+319C>G	N/A	Intron Variant
RNF17 transcript variant X11	XM_047430488.1:c.4307+319… XM_047430488.1:c.4307+319C>G	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	C=	G	T
GRCh38.p14 chr 13	NC_000013.11:g.24874568=	NC_000013.11:g.24874568C>G	NC_000013.11:g.24874568C>T
GRCh37.p13 chr 13	NC_000013.10:g.25448706=	NC_000013.10:g.25448706C>G	NC_000013.10:g.25448706C>T
RNF17 transcript variant 2	NM_001184993.1:c.4571+319=	NM_001184993.1:c.4571+319C>G	NM_001184993.1:c.4571+319C>T
RNF17 transcript variant 2	NM_001184993.2:c.4571+319=	NM_001184993.2:c.4571+319C>G	NM_001184993.2:c.4571+319C>T
RNF17 transcript variant 1	NM_031277.2:c.4583+319=	NM_031277.2:c.4583+319C>G	NM_031277.2:c.4583+319C>T
RNF17 transcript variant 1	NM_031277.3:c.4583+319=	NM_031277.3:c.4583+319C>G	NM_031277.3:c.4583+319C>T
RNF17 transcript variant X1	XM_005266472.1:c.4772+319=	XM_005266472.1:c.4772+319C>G	XM_005266472.1:c.4772+319C>T
RNF17 transcript variant X2	XM_005266473.1:c.4643+319=	XM_005266473.1:c.4643+319C>G	XM_005266473.1:c.4643+319C>T
RNF17 transcript variant X3	XM_005266474.1:c.4400+319=	XM_005266474.1:c.4400+319C>G	XM_005266474.1:c.4400+319C>T
RNF17 transcript variant X5	XM_006719846.4:c.4790+319=	XM_006719846.4:c.4790+319C>G	XM_006719846.4:c.4790+319C>T
RNF17 transcript variant X6	XM_006719849.3:c.4730+319=	XM_006719849.3:c.4730+319C>G	XM_006719849.3:c.4730+319C>T
RNF17 transcript variant X1	XM_011535152.3:c.4811+319=	XM_011535152.3:c.4811+319C>G	XM_011535152.3:c.4811+319C>T
RNF17 transcript variant X3	XM_011535155.3:c.4811+319=	XM_011535155.3:c.4811+319C>G	XM_011535155.3:c.4811+319C>T
RNF17 transcript variant X2	XM_011535156.3:c.4811+319=	XM_011535156.3:c.4811+319C>G	XM_011535156.3:c.4811+319C>T
RNF17 transcript variant X4	XM_011535157.3:c.4799+319=	XM_011535157.3:c.4799+319C>G	XM_011535157.3:c.4799+319C>T
RNF17 transcript variant X7	XM_011535158.3:c.4685+319=	XM_011535158.3:c.4685+319C>G	XM_011535158.3:c.4685+319C>T
RNF17 transcript variant X8	XM_011535159.3:c.4664+319=	XM_011535159.3:c.4664+319C>G	XM_011535159.3:c.4664+319C>T
RNF17 transcript variant X9	XM_011535160.3:c.4652+319=	XM_011535160.3:c.4652+319C>G	XM_011535160.3:c.4652+319C>T
RNF17 transcript variant X12	XM_011535162.2:c.4208+319=	XM_011535162.2:c.4208+319C>G	XM_011535162.2:c.4208+319C>T
RNF17 transcript variant X13	XM_011535163.2:c.3497+319=	XM_011535163.2:c.3497+319C>G	XM_011535163.2:c.3497+319C>T
RNF17 transcript variant X14	XM_011535164.3:c.2381+319=	XM_011535164.3:c.2381+319C>G	XM_011535164.3:c.2381+319C>T
RNF17 transcript variant X10	XM_017020676.2:c.4547+319=	XM_017020676.2:c.4547+319C>G	XM_017020676.2:c.4547+319C>T
RNF17 transcript variant X15	XM_047430486.1:c.4811+319=	XM_047430486.1:c.4811+319C>G	XM_047430486.1:c.4811+319C>T
RNF17 transcript variant X11	XM_047430488.1:c.4307+319=	XM_047430488.1:c.4307+319C>G	XM_047430488.1:c.4307+319C>T

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#.

65 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss13168719	Dec 05, 2003 (119)
2	BCMHGSC_JDW	ss89538430	Mar 24, 2008 (129)
3	HUMANGENOME_JCVI	ss97143078	Feb 03, 2009 (130)
4	BGI	ss103103340	Dec 01, 2009 (131)
5	1000GENOMES	ss114423750	Jan 25, 2009 (130)
6	ENSEMBL	ss143616400	Dec 01, 2009 (131)
7	COMPLETE_GENOMICS	ss167722423	Jul 04, 2010 (132)
8	COMPLETE_GENOMICS	ss168982710	Jul 04, 2010 (132)
9	COMPLETE_GENOMICS	ss170888223	Jul 04, 2010 (132)
10	1000GENOMES	ss226082160	Jul 14, 2010 (132)
11	1000GENOMES	ss236178177	Jul 15, 2010 (132)
12	1000GENOMES	ss242688655	Jul 15, 2010 (132)
13	BL	ss254858138	May 09, 2011 (134)
14	GMI	ss281641024	May 04, 2012 (137)
15	PJP	ss291558295	May 09, 2011 (134)
16	TISHKOFF	ss563552575	Apr 25, 2013 (138)
17	SSMP	ss659146987	Apr 25, 2013 (138)
18	EVA-GONL	ss990196788	Aug 21, 2014 (142)
19	JMKIDD_LAB	ss1078940486	Aug 21, 2014 (142)
20	1000GENOMES	ss1347508243	Aug 21, 2014 (142)
21	DDI	ss1427129789	Apr 01, 2015 (144)
22	EVA_UK10K_ALSPAC	ss1629896717	Apr 01, 2015 (144)
23	EVA_DECODE	ss1642302197	Apr 01, 2015 (144)
24	EVA_UK10K_TWINSUK	ss1672890750	Apr 01, 2015 (144)
25	HAMMER_LAB	ss1807527663	Sep 08, 2015 (146)
26	WEILL_CORNELL_DGM	ss1933565184	Feb 12, 2016 (147)
27	GENOMED	ss1967735588	Jul 19, 2016 (147)
28	JJLAB	ss2027537249	Sep 14, 2016 (149)
29	USC_VALOUEV	ss2155901254	Dec 20, 2016 (150)
30	HUMAN_LONGEVITY	ss2194881561	Dec 20, 2016 (150)
31	SYSTEMSBIOZJU	ss2628256262	Nov 08, 2017 (151)
32	GRF	ss2700273021	Nov 08, 2017 (151)
33	GNOMAD	ss2917636774	Nov 08, 2017 (151)
34	SWEGEN	ss3010727385	Nov 08, 2017 (151)
35	BIOINF_KMB_FNS_UNIBA	ss3027583594	Nov 08, 2017 (151)
36	CSHL	ss3350367193	Nov 08, 2017 (151)
37	URBANLAB	ss3649988878	Oct 12, 2018 (152)
38	EGCUT_WGS	ss3677990034	Jul 13, 2019 (153)
39	EVA_DECODE	ss3694933051	Jul 13, 2019 (153)
40	ACPOP	ss3739585862	Jul 13, 2019 (153)
41	EVA	ss3751240370	Jul 13, 2019 (153)
42	PACBIO	ss3787405379	Jul 13, 2019 (153)
43	PACBIO	ss3792479158	Jul 13, 2019 (153)
44	PACBIO	ss3797362866	Jul 13, 2019 (153)
45	KHV_HUMAN_GENOMES	ss3816571293	Jul 13, 2019 (153)
46	EVA	ss3833450414	Apr 27, 2020 (154)
47	EVA	ss3840301199	Apr 27, 2020 (154)
48	EVA	ss3845785694	Apr 27, 2020 (154)
49	SGDP_PRJ	ss3879600838	Apr 27, 2020 (154)
50	KRGDB	ss3928418772	Apr 27, 2020 (154)
51	KOGIC	ss3973214888	Apr 27, 2020 (154)
52	TOPMED	ss4940059792	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5209193397	Apr 26, 2021 (155)
54	1000G_HIGH_COVERAGE	ss5293108939	Oct 16, 2022 (156)
55	EVA	ss5409629020	Oct 16, 2022 (156)
56	HUGCELL_USP	ss5487534248	Oct 16, 2022 (156)
57	EVA	ss5510909142	Oct 16, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5591749096	Oct 16, 2022 (156)
59	SANFORD_IMAGENETICS	ss5654408545	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5760839393	Oct 16, 2022 (156)
61	YY_MCH	ss5813953679	Oct 16, 2022 (156)
62	EVA	ss5839226834	Oct 16, 2022 (156)
63	EVA	ss5850649250	Oct 16, 2022 (156)
64	EVA	ss5924383732	Oct 16, 2022 (156)
65	EVA	ss5945813426	Oct 16, 2022 (156)
66	1000Genomes	NC_000013.10 - 25448706	Oct 12, 2018 (152)
67	1000Genomes_30x	NC_000013.11 - 24874568	Oct 16, 2022 (156)
68	The Avon Longitudinal Study of Parents and Children	NC_000013.10 - 25448706	Oct 12, 2018 (152)
69	Genetic variation in the Estonian population	NC_000013.10 - 25448706	Oct 12, 2018 (152)
70	gnomAD - Genomes	NC_000013.11 - 24874568	Apr 26, 2021 (155)
71	Genome of the Netherlands Release 5	NC_000013.10 - 25448706	Apr 27, 2020 (154)
72	KOREAN population from KRGDB	NC_000013.10 - 25448706	Apr 27, 2020 (154)
73	Korean Genome Project	NC_000013.11 - 24874568	Apr 27, 2020 (154)
74	Northern Sweden	NC_000013.10 - 25448706	Jul 13, 2019 (153)
75	Qatari	NC_000013.10 - 25448706	Apr 27, 2020 (154)
76	SGDP_PRJ	NC_000013.10 - 25448706	Apr 27, 2020 (154)
77	Siberian	NC_000013.10 - 25448706	Apr 27, 2020 (154)
78	8.3KJPN	NC_000013.10 - 25448706	Apr 26, 2021 (155)
79	14KJPN	NC_000013.11 - 24874568	Oct 16, 2022 (156)
80	TopMed	NC_000013.11 - 24874568	Apr 26, 2021 (155)
81	UK 10K study - Twins	NC_000013.10 - 25448706	Oct 12, 2018 (152)
82	A Vietnamese Genetic Variation Database	NC_000013.10 - 25448706	Jul 13, 2019 (153)
83	ALFA	NC_000013.11 - 24874568	Apr 26, 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
35596166, ss3928418772	NC_000013.10:25448705:C:G	NC_000013.11:24874567:C:G	(self)
ss89538430, ss114423750, ss167722423, ss168982710, ss170888223, ss254858138, ss281641024, ss291558295, ss1642302197	NC_000013.9:24346705:C:T	NC_000013.11:24874567:C:T	(self)
60352147, 33516943, 23728282, 14954185, 35596166, 12870727, 15607114, 31617818, 8417608, 67162704, 33516943, 7434950, ss226082160, ss236178177, ss242688655, ss563552575, ss659146987, ss990196788, ss1078940486, ss1347508243, ss1427129789, ss1629896717, ss1672890750, ss1807527663, ss1933565184, ss1967735588, ss2027537249, ss2155901254, ss2628256262, ss2700273021, ss2917636774, ss3010727385, ss3350367193, ss3677990034, ss3739585862, ss3751240370, ss3787405379, ss3792479158, ss3797362866, ss3833450414, ss3840301199, ss3879600838, ss3928418772, ss5209193397, ss5409629020, ss5510909142, ss5654408545, ss5839226834, ss5945813426	NC_000013.10:25448705:C:T	NC_000013.11:24874567:C:T	(self)
79275031, 425603814, 29592889, 94676497, 155605450, 7569617251, ss2194881561, ss3027583594, ss3649988878, ss3694933051, ss3816571293, ss3845785694, ss3973214888, ss4940059792, ss5293108939, ss5487534248, ss5591749096, ss5760839393, ss5813953679, ss5850649250, ss5924383732	NC_000013.11:24874567:C:T	NC_000013.11:24874567:C:T	(self)
ss13168719	NT_009799.12:6428705:C:T	NC_000013.11:24874567:C:T	(self)
ss97143078, ss103103340, ss143616400	NT_024524.14:6428705:C:T	NC_000013.11:24874567:C:T	(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 rs9511494

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

rs9511494