Name: rs547749
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.

rs547749

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:217011 (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: T>C / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.058963 (15607/264690, TOPMED)
G=0.02757 (1193/43276, ALFA)
G=0.00004 (1/28258, 14KJPN) (+ 13 more)
G=0.00006 (1/16758, 8.3KJPN)
G=0.0657 (421/6404, 1000G_30x)
G=0.0649 (325/5008, 1000G)
G=0.0025 (11/4480, Estonian)
G=0.0036 (14/3854, ALSPAC)
G=0.0032 (12/3708, TWINSUK)
G=0.1338 (193/1442, HapMap)
G=0.011 (11/998, GoNL)
G=0.006 (4/626, Chileans)
G=0.015 (9/600, NorthernSweden)
G=0.065 (14/216, Qatari)
G=0.005 (1/216, Vietnamese)
T=0.38 (13/34, SGDP_PRJ)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SIRT3 : 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	43276	T=0.97243	C=0.00000, G=0.02757
European	Sub	29918	T=0.99609	C=0.00000, G=0.00391
African	Sub	7512	T=0.8675	C=0.0000, G=0.1325
African Others	Sub	240	T=0.858	C=0.000, G=0.142
African American	Sub	7272	T=0.8678	C=0.0000, G=0.1322
Asian	Sub	486	T=1.000	C=0.000, G=0.000
East Asian	Sub	388	T=1.000	C=0.000, G=0.000
Other Asian	Sub	98	T=1.00	C=0.00, G=0.00
Latin American 1	Sub	558	T=0.964	C=0.000, G=0.036
Latin American 2	Sub	964	T=0.994	C=0.000, G=0.006
South Asian	Sub	172	T=0.983	C=0.000, G=0.017
Other	Sub	3666	T=0.9858	C=0.0000, G=0.0142

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=0.941037	G=0.058963
Allele Frequency Aggregator	Total	Global	43276	T=0.97243	C=0.00000, G=0.02757
Allele Frequency Aggregator	European	Sub	29918	T=0.99609	C=0.00000, G=0.00391
Allele Frequency Aggregator	African	Sub	7512	T=0.8675	C=0.0000, G=0.1325
Allele Frequency Aggregator	Other	Sub	3666	T=0.9858	C=0.0000, G=0.0142
Allele Frequency Aggregator	Latin American 2	Sub	964	T=0.994	C=0.000, G=0.006
Allele Frequency Aggregator	Latin American 1	Sub	558	T=0.964	C=0.000, G=0.036
Allele Frequency Aggregator	Asian	Sub	486	T=1.000	C=0.000, G=0.000
Allele Frequency Aggregator	South Asian	Sub	172	T=0.983	C=0.000, G=0.017
14KJPN	JAPANESE	Study-wide	28258	T=0.99996	G=0.00004
8.3KJPN	JAPANESE	Study-wide	16758	T=0.99994	G=0.00006
1000Genomes_30x	Global	Study-wide	6404	T=0.9343	G=0.0657
1000Genomes_30x	African	Sub	1786	T=0.7912	G=0.2088
1000Genomes_30x	Europe	Sub	1266	T=0.9945	G=0.0055
1000Genomes_30x	South Asian	Sub	1202	T=0.9884	G=0.0116
1000Genomes_30x	East Asian	Sub	1170	T=0.9983	G=0.0017
1000Genomes_30x	American	Sub	980	T=0.974	G=0.026
1000Genomes	Global	Study-wide	5008	T=0.9351	G=0.0649
1000Genomes	African	Sub	1322	T=0.7799	G=0.2201
1000Genomes	East Asian	Sub	1008	T=0.9980	G=0.0020
1000Genomes	Europe	Sub	1006	T=0.9960	G=0.0040
1000Genomes	South Asian	Sub	978	T=0.988	G=0.012
1000Genomes	American	Sub	694	T=0.977	G=0.023
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.9975	G=0.0025
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.9964	G=0.0036
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.9968	G=0.0032
HapMap	Global	Study-wide	1442	T=0.8662	G=0.1338
HapMap	African	Sub	692	T=0.751	G=0.249
HapMap	American	Sub	660	T=0.968	G=0.032
HapMap	Asian	Sub	90	T=1.00	G=0.00
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.989	G=0.011
Chileans	Chilean	Study-wide	626	T=0.994	G=0.006
Northern Sweden	ACPOP	Study-wide	600	T=0.985	G=0.015
Qatari	Global	Study-wide	216	T=0.935	G=0.065
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.995	G=0.005
SGDP_PRJ	Global	Study-wide	34	T=0.38	G=0.62

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 11	NC_000011.10:g.217011T>C
GRCh38.p14 chr 11	NC_000011.10:g.217011T>G
GRCh37.p13 chr 11	NC_000011.9:g.217011T>C
GRCh37.p13 chr 11	NC_000011.9:g.217011T>G

Gene: SIRT3, sirtuin 3 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SIRT3 transcript variant 2	NM_001017524.3:c.754-293A… NM_001017524.3:c.754-293A>G	N/A	Intron Variant
SIRT3 transcript variant 3	NM_001370310.1:c.1234-293… NM_001370310.1:c.1234-293A>G	N/A	Intron Variant
SIRT3 transcript variant 4	NM_001370312.1:c.1042-293… NM_001370312.1:c.1042-293A>G	N/A	Intron Variant
SIRT3 transcript variant 5	NM_001370314.1:c.1018-293… NM_001370314.1:c.1018-293A>G	N/A	Intron Variant
SIRT3 transcript variant 6	NM_001370315.1:c.937-293A… NM_001370315.1:c.937-293A>G	N/A	Intron Variant
SIRT3 transcript variant 7	NM_001370316.1:c.508-293A… NM_001370316.1:c.508-293A>G	N/A	Intron Variant
SIRT3 transcript variant 8	NM_001370317.1:c.364-293A… NM_001370317.1:c.364-293A>G	N/A	Intron Variant
SIRT3 transcript variant 9	NM_001370318.1:c.754-293A… NM_001370318.1:c.754-293A>G	N/A	Intron Variant
SIRT3 transcript variant 10	NM_001370319.1:c.754-293A… NM_001370319.1:c.754-293A>G	N/A	Intron Variant
SIRT3 transcript variant 11	NM_001370320.1:c.754-293A… NM_001370320.1:c.754-293A>G	N/A	Intron Variant
SIRT3 transcript variant 12	NM_001370321.1:c.808-293A… NM_001370321.1:c.808-293A>G	N/A	Intron Variant
SIRT3 transcript variant 13	NM_001370322.1:c.808-293A… NM_001370322.1:c.808-293A>G	N/A	Intron Variant
SIRT3 transcript variant 14	NM_001370323.1:c.808-293A… NM_001370323.1:c.808-293A>G	N/A	Intron Variant
SIRT3 transcript variant 15	NM_001370324.1:c.544-293A… NM_001370324.1:c.544-293A>G	N/A	Intron Variant
SIRT3 transcript variant 16	NM_001370325.1:c.544-293A… NM_001370325.1:c.544-293A>G	N/A	Intron Variant
SIRT3 transcript variant 1	NM_012239.6:c.1180-293A>G	N/A	Intron Variant
SIRT3 transcript variant 17	NR_163386.1:n.	N/A	Intron Variant
SIRT3 transcript variant 18	NR_163387.1:n.	N/A	Intron Variant
SIRT3 transcript variant 19	NR_163388.1:n.	N/A	Intron Variant
SIRT3 transcript variant 20	NR_163389.1:n.	N/A	Intron Variant
SIRT3 transcript variant 21	NR_163390.1:n.	N/A	Intron Variant
SIRT3 transcript variant 22	NR_163391.1:n.	N/A	Intron Variant
SIRT3 transcript variant 23	NR_163392.1:n.	N/A	Intron Variant
SIRT3 transcript variant 24	NR_163393.1:n.	N/A	Intron Variant
SIRT3 transcript variant 25	NR_163394.1:n.	N/A	Intron Variant
SIRT3 transcript variant 26	NR_163395.1:n.	N/A	Intron Variant
SIRT3 transcript variant 27	NR_163396.1:n.	N/A	Intron Variant
SIRT3 transcript variant 28	NR_163397.1:n.	N/A	Intron Variant
SIRT3 transcript variant 29	NR_163398.1:n.	N/A	Intron Variant
SIRT3 transcript variant 30	NR_163399.1:n.	N/A	Intron Variant
SIRT3 transcript variant 31	NR_163400.1:n.	N/A	Intron Variant
SIRT3 transcript variant 32	NR_163401.1:n.	N/A	Intron Variant
SIRT3 transcript variant 33	NR_163402.1:n.	N/A	Intron Variant
SIRT3 transcript variant X3	XM_011519956.3:c.808-293A… XM_011519956.3:c.808-293A>G	N/A	Intron Variant
SIRT3 transcript variant X2	XM_011519957.3:c.808-293A… XM_011519957.3:c.808-293A>G	N/A	Intron Variant
SIRT3 transcript variant X4	XM_017017431.2:c.808-293A… XM_017017431.2:c.808-293A>G	N/A	Intron Variant
SIRT3 transcript variant X5	XM_047426677.1:c.754-293A… XM_047426677.1:c.754-293A>G	N/A	Intron Variant
SIRT3 transcript variant X1	XR_007062467.1:n.	N/A	Genic Downstream 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=	C	G
GRCh38.p14 chr 11	NC_000011.10:g.217011=	NC_000011.10:g.217011T>C	NC_000011.10:g.217011T>G
GRCh37.p13 chr 11	NC_000011.9:g.217011=	NC_000011.9:g.217011T>C	NC_000011.9:g.217011T>G
SIRT3 transcript variant 2	NM_001017524.2:c.754-293=	NM_001017524.2:c.754-293A>G	NM_001017524.2:c.754-293A>C
SIRT3 transcript variant 2	NM_001017524.3:c.754-293=	NM_001017524.3:c.754-293A>G	NM_001017524.3:c.754-293A>C
SIRT3 transcript variant 3	NM_001370310.1:c.1234-293=	NM_001370310.1:c.1234-293A>G	NM_001370310.1:c.1234-293A>C
SIRT3 transcript variant 4	NM_001370312.1:c.1042-293=	NM_001370312.1:c.1042-293A>G	NM_001370312.1:c.1042-293A>C
SIRT3 transcript variant 5	NM_001370314.1:c.1018-293=	NM_001370314.1:c.1018-293A>G	NM_001370314.1:c.1018-293A>C
SIRT3 transcript variant 6	NM_001370315.1:c.937-293=	NM_001370315.1:c.937-293A>G	NM_001370315.1:c.937-293A>C
SIRT3 transcript variant 7	NM_001370316.1:c.508-293=	NM_001370316.1:c.508-293A>G	NM_001370316.1:c.508-293A>C
SIRT3 transcript variant 8	NM_001370317.1:c.364-293=	NM_001370317.1:c.364-293A>G	NM_001370317.1:c.364-293A>C
SIRT3 transcript variant 9	NM_001370318.1:c.754-293=	NM_001370318.1:c.754-293A>G	NM_001370318.1:c.754-293A>C
SIRT3 transcript variant 10	NM_001370319.1:c.754-293=	NM_001370319.1:c.754-293A>G	NM_001370319.1:c.754-293A>C
SIRT3 transcript variant 11	NM_001370320.1:c.754-293=	NM_001370320.1:c.754-293A>G	NM_001370320.1:c.754-293A>C
SIRT3 transcript variant 12	NM_001370321.1:c.808-293=	NM_001370321.1:c.808-293A>G	NM_001370321.1:c.808-293A>C
SIRT3 transcript variant 13	NM_001370322.1:c.808-293=	NM_001370322.1:c.808-293A>G	NM_001370322.1:c.808-293A>C
SIRT3 transcript variant 14	NM_001370323.1:c.808-293=	NM_001370323.1:c.808-293A>G	NM_001370323.1:c.808-293A>C
SIRT3 transcript variant 15	NM_001370324.1:c.544-293=	NM_001370324.1:c.544-293A>G	NM_001370324.1:c.544-293A>C
SIRT3 transcript variant 16	NM_001370325.1:c.544-293=	NM_001370325.1:c.544-293A>G	NM_001370325.1:c.544-293A>C
SIRT3 transcript variant 1	NM_012239.5:c.1180-293=	NM_012239.5:c.1180-293A>G	NM_012239.5:c.1180-293A>C
SIRT3 transcript variant 1	NM_012239.6:c.1180-293=	NM_012239.6:c.1180-293A>G	NM_012239.6:c.1180-293A>C
SIRT3 transcript variant X1	XM_005252835.1:c.1234-293=	XM_005252835.1:c.1234-293A>G	XM_005252835.1:c.1234-293A>C
SIRT3 transcript variant X2	XM_005252836.1:c.1042-293=	XM_005252836.1:c.1042-293A>G	XM_005252836.1:c.1042-293A>C
SIRT3 transcript variant X3	XM_005252837.1:c.1018-293=	XM_005252837.1:c.1018-293A>G	XM_005252837.1:c.1018-293A>C
SIRT3 transcript variant X4	XM_005252838.1:c.937-293=	XM_005252838.1:c.937-293A>G	XM_005252838.1:c.937-293A>C
SIRT3 transcript variant X3	XM_011519956.3:c.808-293=	XM_011519956.3:c.808-293A>G	XM_011519956.3:c.808-293A>C
SIRT3 transcript variant X2	XM_011519957.3:c.808-293=	XM_011519957.3:c.808-293A>G	XM_011519957.3:c.808-293A>C
SIRT3 transcript variant X4	XM_017017431.2:c.808-293=	XM_017017431.2:c.808-293A>G	XM_017017431.2:c.808-293A>C
SIRT3 transcript variant X5	XM_047426677.1:c.754-293=	XM_047426677.1:c.754-293A>G	XM_047426677.1:c.754-293A>C

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, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss718626	Aug 11, 2000 (83)
2	PERLEGEN	ss23627931	Sep 20, 2004 (123)
3	AFFY	ss76487145	Dec 06, 2007 (129)
4	KRIBB_YJKIM	ss104820338	Feb 03, 2009 (130)
5	ILLUMINA-UK	ss118437439	Feb 14, 2009 (130)
6	ILLUMINA	ss160741924	Dec 01, 2009 (131)
7	BUSHMAN	ss202252806	Jul 04, 2010 (132)
8	1000GENOMES	ss225042567	Jul 14, 2010 (132)
9	ILLUMINA	ss482155685	Sep 08, 2015 (146)
10	TISHKOFF	ss562325737	Apr 25, 2013 (138)
11	SSMP	ss657640352	Apr 25, 2013 (138)
12	EVA-GONL	ss988111672	Aug 21, 2014 (142)
13	JMKIDD_LAB	ss1077435694	Aug 21, 2014 (142)
14	1000GENOMES	ss1339765067	Aug 21, 2014 (142)
15	EVA_DECODE	ss1597790509	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1625814873	Apr 01, 2015 (144)
17	EVA_UK10K_TWINSUK	ss1668808906	Apr 01, 2015 (144)
18	EVA_SVP	ss1713226312	Apr 01, 2015 (144)
19	HAMMER_LAB	ss1806651649	Sep 08, 2015 (146)
20	WEILL_CORNELL_DGM	ss1931471737	Feb 12, 2016 (147)
21	JJLAB	ss2026476455	Sep 14, 2016 (149)
22	HUMAN_LONGEVITY	ss2179516891	Dec 20, 2016 (150)
23	GNOMAD	ss2895338085	Nov 08, 2017 (151)
24	SWEGEN	ss3007442763	Nov 08, 2017 (151)
25	ILLUMINA	ss3636119003	Oct 12, 2018 (152)
26	EGCUT_WGS	ss3674852817	Jul 13, 2019 (153)
27	EVA_DECODE	ss3691039583	Jul 13, 2019 (153)
28	ACPOP	ss3737838368	Jul 13, 2019 (153)
29	EVA	ss3748832379	Jul 13, 2019 (153)
30	KHV_HUMAN_GENOMES	ss3814182460	Jul 13, 2019 (153)
31	EVA	ss3832427712	Apr 26, 2020 (154)
32	SGDP_PRJ	ss3875442968	Apr 26, 2020 (154)
33	TOPMED	ss4872332384	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5200276463	Apr 26, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5286090112	Oct 16, 2022 (156)
36	EVA	ss5397184222	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5481443886	Oct 16, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5581067061	Oct 16, 2022 (156)
39	SANFORD_IMAGENETICS	ss5650452742	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5746909995	Oct 16, 2022 (156)
41	EVA	ss5836134207	Oct 16, 2022 (156)
42	EVA	ss5918489900	Oct 16, 2022 (156)
43	EVA	ss5941763544	Oct 16, 2022 (156)
44	1000Genomes	NC_000011.9 - 217011	Oct 12, 2018 (152)
45	1000Genomes_30x	NC_000011.10 - 217011	Oct 16, 2022 (156)
46	The Avon Longitudinal Study of Parents and Children	NC_000011.9 - 217011	Oct 12, 2018 (152)
47	Chileans	NC_000011.9 - 217011	Apr 26, 2020 (154)
48	Genetic variation in the Estonian population	NC_000011.9 - 217011	Oct 12, 2018 (152)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368914232 (NC_000011.10:217010:T:C 1/140250) Row 368914233 (NC_000011.10:217010:T:G 8002/140236)	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368914232 (NC_000011.10:217010:T:C 1/140250) Row 368914233 (NC_000011.10:217010:T:G 8002/140236)	-	Apr 26, 2021 (155)
51	Genome of the Netherlands Release 5	NC_000011.9 - 217011	Apr 26, 2020 (154)
52	HapMap	NC_000011.10 - 217011	Apr 26, 2020 (154)
53	Northern Sweden	NC_000011.9 - 217011	Jul 13, 2019 (153)
54	Qatari	NC_000011.9 - 217011	Apr 26, 2020 (154)
55	SGDP_PRJ	NC_000011.9 - 217011	Apr 26, 2020 (154)
56	8.3KJPN	NC_000011.9 - 217011	Apr 26, 2021 (155)
57	14KJPN	NC_000011.10 - 217011	Oct 16, 2022 (156)
58	TopMed	NC_000011.10 - 217011	Apr 26, 2021 (155)
59	UK 10K study - Twins	NC_000011.9 - 217011	Oct 12, 2018 (152)
60	A Vietnamese Genetic Variation Database	NC_000011.9 - 217011	Jul 13, 2019 (153)
61	ALFA	NC_000011.10 - 217011	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).

Associated ID	History Updated (Build)
rs17155834	Oct 08, 2004 (123)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss2895338085	NC_000011.9:217010:T:C	NC_000011.10:217010:T:C	(self)
1595590549	NC_000011.10:217010:T:C	NC_000011.10:217010:T:C	(self)
ss76487145, ss118437439, ss160741924, ss202252806, ss1597790509, ss1713226312	NC_000011.8:207010:T:G	NC_000011.10:217010:T:G	(self)
52235962, 29024140, 66480, 20591065, 12937081, 11123233, 13513667, 27459948, 58245770, 29024140, 6442123, ss225042567, ss482155685, ss562325737, ss657640352, ss988111672, ss1077435694, ss1339765067, ss1625814873, ss1668808906, ss1806651649, ss1931471737, ss2026476455, ss2895338085, ss3007442763, ss3636119003, ss3674852817, ss3737838368, ss3748832379, ss3832427712, ss3875442968, ss5200276463, ss5397184222, ss5650452742, ss5836134207, ss5941763544	NC_000011.9:217010:T:G	NC_000011.10:217010:T:G	(self)
68592996, 531074, 80747099, 87878040, 1595590549, ss2179516891, ss3691039583, ss3814182460, ss4872332384, ss5286090112, ss5481443886, ss5581067061, ss5746909995, ss5918489900	NC_000011.10:217010:T:G	NC_000011.10:217010:T:G	(self)
ss718626, ss23627931, ss104820338	NT_009237.18:157010:T:G	NC_000011.10:217010:T:G	(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 rs547749

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

rs547749