Name: rs5751738
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.

rs5751738

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:23803488 (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: G>A / G>C / G>T
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.085179 (22546/264690, TOPMED)
G=0.075979 (10657/140262, GnomAD)
G=0.34029 (9616/28258, 14KJPN) (+ 15 more)
G=0.33455 (5607/16760, 8.3KJPN)
G=0.0801 (575/7182, ALFA)
G=0.1309 (838/6404, 1000G_30x)
G=0.1332 (667/5008, 1000G)
G=0.0670 (300/4480, Estonian)
G=0.0701 (270/3854, ALSPAC)
G=0.0618 (229/3708, TWINSUK)
G=0.3222 (944/2930, KOREAN)
G=0.060 (60/998, GoNL)
G=0.057 (34/600, NorthernSweden)
G=0.165 (88/534, MGP)
G=0.125 (65/520, SGDP_PRJ)
G=0.097 (21/216, Qatari)
G=0.264 (56/212, Vietnamese)
G=0.09 (5/56, Siberian)

Clinical Significance: Reported in ClinVar
Gene : Consequence: SMARCB1 : 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	7182	G=0.0801	A=0.0000, C=0.9199, T=0.0000
European	Sub	6756	G=0.0749	A=0.0000, C=0.9251, T=0.0000
African	Sub	160	G=0.138	A=0.000, C=0.863, T=0.000
African Others	Sub	8	G=0.5	A=0.0, C=0.5, T=0.0
African American	Sub	152	G=0.118	A=0.000, C=0.882, T=0.000
Asian	Sub	6	G=0.3	A=0.0, C=0.7, T=0.0
East Asian	Sub	4	G=0.5	A=0.0, C=0.5, T=0.0
Other Asian	Sub	2	G=0.0	A=0.0, C=1.0, T=0.0
Latin American 1	Sub	0	G=0	A=0, C=0, T=0
Latin American 2	Sub	20	G=1.00	A=0.00, C=0.00, T=0.00
South Asian	Sub	6	G=0.3	A=0.0, C=0.7, T=0.0
Other	Sub	234	G=0.098	A=0.000, C=0.902, T=0.000

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	G=0.085179	C=0.914821
gnomAD - Genomes	Global	Study-wide	140262	G=0.075979	C=0.924021
gnomAD - Genomes	European	Sub	75964	G=0.07134	C=0.92866
gnomAD - Genomes	African	Sub	42042	G=0.06527	C=0.93473
gnomAD - Genomes	American	Sub	13656	G=0.09058	C=0.90942
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	G=0.0689	C=0.9311
gnomAD - Genomes	East Asian	Sub	3122	G=0.2687	C=0.7313
gnomAD - Genomes	Other	Sub	2154	G=0.0877	C=0.9123
14KJPN	JAPANESE	Study-wide	28258	G=0.34029	C=0.65971
8.3KJPN	JAPANESE	Study-wide	16760	G=0.33455	C=0.66545
Allele Frequency Aggregator	Total	Global	7182	G=0.0801	A=0.0000, C=0.9199, T=0.0000
Allele Frequency Aggregator	European	Sub	6756	G=0.0749	A=0.0000, C=0.9251, T=0.0000
Allele Frequency Aggregator	Other	Sub	234	G=0.098	A=0.000, C=0.902, T=0.000
Allele Frequency Aggregator	African	Sub	160	G=0.138	A=0.000, C=0.863, T=0.000
Allele Frequency Aggregator	Latin American 2	Sub	20	G=1.00	A=0.00, C=0.00, T=0.00
Allele Frequency Aggregator	South Asian	Sub	6	G=0.3	A=0.0, C=0.7, T=0.0
Allele Frequency Aggregator	Asian	Sub	6	G=0.3	A=0.0, C=0.7, T=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	G=0	A=0, C=0, T=0
1000Genomes_30x	Global	Study-wide	6404	G=0.1309	C=0.8688, T=0.0003
1000Genomes_30x	African	Sub	1786	G=0.0694	C=0.9295, T=0.0011
1000Genomes_30x	Europe	Sub	1266	G=0.0608	C=0.9392, T=0.0000
1000Genomes_30x	South Asian	Sub	1202	G=0.1814	C=0.8186, T=0.0000
1000Genomes_30x	East Asian	Sub	1170	G=0.2675	C=0.7325, T=0.0000
1000Genomes_30x	American	Sub	980	G=0.108	C=0.892, T=0.000
1000Genomes	Global	Study-wide	5008	G=0.1332	C=0.8668
1000Genomes	African	Sub	1322	G=0.0651	C=0.9349
1000Genomes	East Asian	Sub	1008	G=0.2649	C=0.7351
1000Genomes	Europe	Sub	1006	G=0.0567	C=0.9433
1000Genomes	South Asian	Sub	978	G=0.187	C=0.813
1000Genomes	American	Sub	694	G=0.107	C=0.893
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.0670	C=0.9330
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.0701	C=0.9299
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.0618	C=0.9382
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.3222	A=0.0000, C=0.6778
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.060	C=0.940
Northern Sweden	ACPOP	Study-wide	600	G=0.057	C=0.943
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	G=0.165	C=0.835
SGDP_PRJ	Global	Study-wide	520	G=0.125	C=0.875
Qatari	Global	Study-wide	216	G=0.097	C=0.903
A Vietnamese Genetic Variation Database	Global	Study-wide	212	G=0.264	C=0.736
Siberian	Global	Study-wide	56	G=0.09	C=0.91

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 22	NC_000022.11:g.23803488G>A
GRCh38.p14 chr 22	NC_000022.11:g.23803488G>C
GRCh38.p14 chr 22	NC_000022.11:g.23803488G>T
GRCh37.p13 chr 22	NC_000022.10:g.24145675G>A
GRCh37.p13 chr 22	NC_000022.10:g.24145675G>C
GRCh37.p13 chr 22	NC_000022.10:g.24145675G>T
SMARCB1 RefSeqGene (LRG_520)	NG_009303.1:g.21526G>A
SMARCB1 RefSeqGene (LRG_520)	NG_009303.1:g.21526G>C
SMARCB1 RefSeqGene (LRG_520)	NG_009303.1:g.21526G>T
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG7	NT_187633.1:g.39850G>A
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG7	NT_187633.1:g.39850G>C
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG7	NT_187633.1:g.39850G>T

Gene: SMARCB1, SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SMARCB1 transcript variant 2	NM_001007468.3:c.601+66G>A	N/A	Intron Variant
SMARCB1 transcript variant 3	NM_001317946.2:c.655+66G>A	N/A	Intron Variant
SMARCB1 transcript variant 4	NM_001362877.2:c.682+66G>A	N/A	Intron Variant
SMARCB1 transcript variant 1	NM_003073.5:c.628+66G>A	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.

Allele: C (allele ID: 1213564 )

ClinVar Accession	Disease Names	Clinical Significance
RCV001595820.3	not provided	Benign

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	G=	A	C	T
GRCh38.p14 chr 22	NC_000022.11:g.23803488=	NC_000022.11:g.23803488G>A	NC_000022.11:g.23803488G>C	NC_000022.11:g.23803488G>T
GRCh37.p13 chr 22	NC_000022.10:g.24145675=	NC_000022.10:g.24145675G>A	NC_000022.10:g.24145675G>C	NC_000022.10:g.24145675G>T
SMARCB1 RefSeqGene (LRG_520)	NG_009303.1:g.21526=	NG_009303.1:g.21526G>A	NG_009303.1:g.21526G>C	NG_009303.1:g.21526G>T
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG7	NT_187633.1:g.39850=	NT_187633.1:g.39850G>A	NT_187633.1:g.39850G>C	NT_187633.1:g.39850G>T
SMARCB1 transcript variant 2	NM_001007468.1:c.601+66=	NM_001007468.1:c.601+66G>A	NM_001007468.1:c.601+66G>C	NM_001007468.1:c.601+66G>T
SMARCB1 transcript variant 2	NM_001007468.3:c.601+66=	NM_001007468.3:c.601+66G>A	NM_001007468.3:c.601+66G>C	NM_001007468.3:c.601+66G>T
SMARCB1 transcript variant 3	NM_001317946.2:c.655+66=	NM_001317946.2:c.655+66G>A	NM_001317946.2:c.655+66G>C	NM_001317946.2:c.655+66G>T
SMARCB1 transcript variant 4	NM_001362877.2:c.682+66=	NM_001362877.2:c.682+66G>A	NM_001362877.2:c.682+66G>C	NM_001362877.2:c.682+66G>T
SMARCB1 transcript variant 1	NM_003073.3:c.628+66=	NM_003073.3:c.628+66G>A	NM_003073.3:c.628+66G>C	NM_003073.3:c.628+66G>T
SMARCB1 transcript variant 1	NM_003073.5:c.628+66=	NM_003073.5:c.628+66G>A	NM_003073.5:c.628+66G>C	NM_003073.5:c.628+66G>T
SMARCB1 transcript variant X1	XM_005261718.1:c.655+66=	XM_005261718.1:c.655+66G>A	XM_005261718.1:c.655+66G>C	XM_005261718.1:c.655+66G>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#.

93 SubSNP, 18 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss7999784	Apr 21, 2003 (114)
2	BCM_SSAHASNP	ss11011265	Jul 11, 2003 (117)
3	SC_SNP	ss13388684	Dec 05, 2003 (119)
4	SSAHASNP	ss21862923	Apr 05, 2004 (121)
5	EGP_SNPS	ss48532394	Mar 13, 2006 (126)
6	KRIBB_YJKIM	ss65828907	Nov 29, 2006 (127)
7	HGSV	ss78621678	Dec 06, 2007 (129)
8	HGSV	ss80460905	Dec 14, 2007 (130)
9	BCMHGSC_JDW	ss91890190	Mar 24, 2008 (129)
10	BGI	ss103846822	Dec 01, 2009 (131)
11	ILLUMINA-UK	ss117372574	Feb 14, 2009 (130)
12	ENSEMBL	ss138340141	Dec 01, 2009 (131)
13	ENSEMBL	ss139733816	Dec 01, 2009 (131)
14	GMI	ss157071616	Dec 01, 2009 (131)
15	COMPLETE_GENOMICS	ss167745600	Jul 04, 2010 (132)
16	COMPLETE_GENOMICS	ss168971550	Jul 04, 2010 (132)
17	COMPLETE_GENOMICS	ss171862527	Jul 04, 2010 (132)
18	BUSHMAN	ss204059756	Jul 04, 2010 (132)
19	BCM-HGSC-SUB	ss208829880	Jul 04, 2010 (132)
20	1000GENOMES	ss212106725	Jul 14, 2010 (132)
21	1000GENOMES	ss228632933	Jul 14, 2010 (132)
22	1000GENOMES	ss238033323	Jul 15, 2010 (132)
23	1000GENOMES	ss244160722	Jul 15, 2010 (132)
24	BL	ss255858489	May 09, 2011 (134)
25	GMI	ss283600816	May 04, 2012 (137)
26	GMI	ss287554486	Apr 25, 2013 (138)
27	PJP	ss292742409	May 09, 2011 (134)
28	TISHKOFF	ss566579178	Apr 25, 2013 (138)
29	SSMP	ss662507494	Apr 25, 2013 (138)
30	EVA-GONL	ss995252860	Aug 21, 2014 (142)
31	JMKIDD_LAB	ss1082590099	Aug 21, 2014 (142)
32	1000GENOMES	ss1366801774	Aug 21, 2014 (142)
33	DDI	ss1429230373	Apr 01, 2015 (144)
34	EVA_UK10K_ALSPAC	ss1639804893	Apr 01, 2015 (144)
35	EVA_UK10K_TWINSUK	ss1682798926	Apr 01, 2015 (144)
36	EVA_DECODE	ss1699321163	Apr 01, 2015 (144)
37	EVA_MGP	ss1711563749	Apr 01, 2015 (144)
38	HAMMER_LAB	ss1809747420	Sep 08, 2015 (146)
39	WEILL_CORNELL_DGM	ss1938819147	Feb 12, 2016 (147)
40	GENOMED	ss1966658583	Feb 12, 2016 (147)
41	JJLAB	ss2030181942	Sep 14, 2016 (149)
42	USC_VALOUEV	ss2158794088	Dec 20, 2016 (150)
43	HUMAN_LONGEVITY	ss2246620671	Dec 20, 2016 (150)
44	SYSTEMSBIOZJU	ss2629589471	Nov 08, 2017 (151)
45	GRF	ss2704542320	Nov 08, 2017 (151)
46	GNOMAD	ss2973353670	Nov 08, 2017 (151)
47	SWEGEN	ss3019150148	Nov 08, 2017 (151)
48	BIOINF_KMB_FNS_UNIBA	ss3028928321	Nov 08, 2017 (151)
49	CSHL	ss3352793543	Nov 08, 2017 (151)
50	OMUKHERJEE_ADBS	ss3646564523	Oct 12, 2018 (152)
51	URBANLAB	ss3651159464	Oct 12, 2018 (152)
52	EGCUT_WGS	ss3685655349	Jul 13, 2019 (153)
53	EVA_DECODE	ss3708011686	Jul 13, 2019 (153)
54	ACPOP	ss3743850197	Jul 13, 2019 (153)
55	EVA	ss3759267529	Jul 13, 2019 (153)
56	PACBIO	ss3788802417	Jul 13, 2019 (153)
57	PACBIO	ss3793672391	Jul 13, 2019 (153)
58	PACBIO	ss3798558775	Jul 13, 2019 (153)
59	KHV_HUMAN_GENOMES	ss3822434812	Jul 13, 2019 (153)
60	EVA	ss3835942753	Apr 27, 2020 (154)
61	EVA	ss3841599827	Apr 27, 2020 (154)
62	EVA	ss3847114190	Apr 27, 2020 (154)
63	SGDP_PRJ	ss3890347577	Apr 27, 2020 (154)
64	KRGDB	ss3940738479	Apr 27, 2020 (154)
65	FSA-LAB	ss3984231799	Apr 26, 2021 (155)
66	EVA	ss3986856576	Apr 26, 2021 (155)
67	VINODS	ss4034756435	Apr 26, 2021 (155)
68	TOPMED	ss5106042885	Apr 26, 2021 (155)
69	TOMMO_GENOMICS	ss5232199343	Apr 26, 2021 (155)
70	CPQ_GEN_INCA	ss5236854562	Apr 26, 2021 (155)
71	CPQ_GEN_INCA	ss5236859211	Apr 26, 2021 (155)
72	EVA	ss5237255319	Apr 26, 2021 (155)
73	1000G_HIGH_COVERAGE	ss5310774681	Oct 16, 2022 (156)
74	1000G_HIGH_COVERAGE	ss5310774682	Oct 16, 2022 (156)
75	EVA	ss5440719738	Oct 16, 2022 (156)
76	HUGCELL_USP	ss5502652832	Oct 16, 2022 (156)
77	EVA	ss5512353535	Oct 16, 2022 (156)
78	1000G_HIGH_COVERAGE	ss5618182554	Oct 16, 2022 (156)
79	EVA	ss5623983293	Oct 16, 2022 (156)
80	EVA	ss5624120977	Oct 16, 2022 (156)
81	SANFORD_IMAGENETICS	ss5664310885	Oct 16, 2022 (156)
82	TOMMO_GENOMICS	ss5793186137	Oct 16, 2022 (156)
83	EVA	ss5800075526	Oct 16, 2022 (156)
84	EVA	ss5800234971	Oct 16, 2022 (156)
85	YY_MCH	ss5818628321	Oct 16, 2022 (156)
86	EVA	ss5821943412	Oct 16, 2022 (156)
87	EVA	ss5848564288	Oct 16, 2022 (156)
88	EVA	ss5853358725	Oct 16, 2022 (156)
89	EVA	ss5881457745	Oct 16, 2022 (156)
90	EVA	ss5936451051	Oct 16, 2022 (156)
91	EVA	ss5959163674	Oct 16, 2022 (156)
92	EVA	ss5981127621	Oct 16, 2022 (156)
93	EVA	ss5981321343	Oct 16, 2022 (156)
94	1000Genomes	NC_000022.10 - 24145675	Oct 12, 2018 (152)
95	1000Genomes_30x	NC_000022.11 - 23803488	Oct 16, 2022 (156)
96	The Avon Longitudinal Study of Parents and Children	NC_000022.10 - 24145675	Oct 12, 2018 (152)
97	Genetic variation in the Estonian population	NC_000022.10 - 24145675	Oct 12, 2018 (152)
98	gnomAD - Genomes	NC_000022.11 - 23803488	Apr 26, 2021 (155)
99	Genome of the Netherlands Release 5	NC_000022.10 - 24145675	Apr 27, 2020 (154)
100	KOREAN population from KRGDB	NC_000022.10 - 24145675	Apr 27, 2020 (154)
101	Medical Genome Project healthy controls from Spanish population	NC_000022.10 - 24145675	Apr 27, 2020 (154)
102	Northern Sweden	NC_000022.10 - 24145675	Jul 13, 2019 (153)
103	Qatari	NC_000022.10 - 24145675	Apr 27, 2020 (154)
104	SGDP_PRJ	NC_000022.10 - 24145675	Apr 27, 2020 (154)
105	Siberian	NC_000022.10 - 24145675	Apr 27, 2020 (154)
106	8.3KJPN	NC_000022.10 - 24145675	Apr 26, 2021 (155)
107	14KJPN	NC_000022.11 - 23803488	Oct 16, 2022 (156)
108	TopMed	NC_000022.11 - 23803488	Apr 26, 2021 (155)
109	UK 10K study - Twins	NC_000022.10 - 24145675	Oct 12, 2018 (152)
110	A Vietnamese Genetic Variation Database	NC_000022.10 - 24145675	Jul 13, 2019 (153)
111	ALFA	NC_000022.11 - 23803488	Apr 26, 2021 (155)
112	ClinVar	RCV001595820.3	Oct 16, 2022 (156)

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)
rs7292555	Aug 27, 2003 (117)
rs57587409	May 23, 2008 (130)
rs117289130	Aug 16, 2010 (132)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
47915873, ss3940738479, ss5936451051	NC_000022.10:24145674:G:A	NC_000022.11:23803487:G:A	(self)
4546353959	NC_000022.11:23803487:G:A	NC_000022.11:23803487:G:A	(self)
ss78621678, ss80460905	NC_000022.8:22470228:G:C	NC_000022.11:23803487:G:C	(self)
ss91890190, ss117372574, ss167745600, ss168971550, ss171862527, ss204059756, ss208829880, ss212106725, ss255858489, ss283600816, ss287554486, ss292742409, ss1699321163	NC_000022.9:22475674:G:C	NC_000022.11:23803487:G:C	(self)
80340278, 44438619, 31393597, 19801380, 47915873, 679509, 17135062, 20861069, 42364557, 11310442, 90168650, 44438619, 9806083, ss228632933, ss238033323, ss244160722, ss566579178, ss662507494, ss995252860, ss1082590099, ss1366801774, ss1429230373, ss1639804893, ss1682798926, ss1711563749, ss1809747420, ss1938819147, ss1966658583, ss2030181942, ss2158794088, ss2629589471, ss2704542320, ss2973353670, ss3019150148, ss3352793543, ss3646564523, ss3685655349, ss3743850197, ss3759267529, ss3788802417, ss3793672391, ss3798558775, ss3835942753, ss3841599827, ss3890347577, ss3940738479, ss3984231799, ss3986856576, ss5232199343, ss5236854562, ss5236859211, ss5440719738, ss5512353535, ss5623983293, ss5624120977, ss5664310885, ss5800075526, ss5800234971, ss5821943412, ss5848564288, ss5936451051, ss5959163674, ss5981127621, ss5981321343	NC_000022.10:24145674:G:C	NC_000022.11:23803487:G:C	(self)
RCV001595820.3, 105708489, 567356652, 127023241, 381151832, 4546353959, ss2246620671, ss3028928321, ss3651159464, ss3708011686, ss3822434812, ss3847114190, ss5106042885, ss5237255319, ss5310774681, ss5502652832, ss5618182554, ss5793186137, ss5818628321, ss5853358725, ss5881457745	NC_000022.11:23803487:G:C	NC_000022.11:23803487:G:C	(self)
ss11011265, ss13388684, ss21862923	NT_011520.9:3536243:G:C	NC_000022.11:23803487:G:C	(self)
ss7999784, ss48532394, ss65828907, ss103846822, ss138340141, ss139733816, ss157071616	NT_011520.12:3536243:G:C	NC_000022.11:23803487:G:C	(self)
ss4034756435	NT_187633.1:39849:G:C	NC_000022.11:23803487:G:C	(self)
105708489, 4546353959, ss5310774682, ss5618182554	NC_000022.11:23803487:G:T	NC_000022.11:23803487:G:T	(self)
ss48532394	NT_011520.12:3536243:G:T	NC_000022.11:23803487:G: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 rs5751738

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

rs5751738