rs6771157

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs6771157(C;C)

Make rs6771157(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

38722372

Gene

SCN10A

is a	snp
is	mentioned by
dbSNP	rs6771157
dbSNP (classic)	rs6771157
ClinGen	rs6771157
ebi	rs6771157
HLI	rs6771157
Exac	rs6771157
Gnomad	rs6771157
Varsome	rs6771157
LitVar	rs6771157
Map	rs6771157
PheGenI	rs6771157
Biobank	rs6771157
1000 genomes	rs6771157
hgdp	rs6771157
ensembl	rs6771157
geneview	rs6771157
scholar	rs6771157
google	rs6771157
pharmgkb	rs6771157
gwascentral	rs6771157
openSNP	rs6771157
23andMe	rs6771157
SNPshot	rs6771157
SNPdbe	rs6771157
MSV3d	rs6771157
GWAS Ctlg	rs6771157

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

[PMID 27725708] The rs6771157 C/G polymorphism in SCN10A is associated with the risk of atrial fibrillation in a Chinese Han population.

ClinVar
Risk	rs6771157(C;C)
Alt	rs6771157(C;C)
Reference	Rs6771157(G;G)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	SCN10A
CLNDBN	not specified
Reversed	0
HGVS	NC_000003.11:g.38763863G>C
CLNSRC
CLNACC	RCV000244131.2,

[PMID 30110000] [Rs17042171 at chromosome 4q25 is associated with atrial fibrillation in the Chinese Han population from the central plains].