rs761117662

Orientation

plus

Stabilized

plus

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

Make rs761117662(C;G)

Make rs761117662(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

38606016

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs761117662
dbSNP (classic)	rs761117662
ClinGen	rs761117662
ebi	rs761117662
HLI	rs761117662
Exac	rs761117662
Gnomad	rs761117662
Varsome	rs761117662
LitVar	rs761117662
Map	rs761117662
PheGenI	rs761117662
Biobank	rs761117662
1000 genomes	rs761117662
hgdp	rs761117662
ensembl	rs761117662
geneview	rs761117662
scholar	rs761117662
google	rs761117662
pharmgkb	rs761117662
gwascentral	rs761117662
openSNP	rs761117662
23andMe	rs761117662
SNPshot	rs761117662
SNPdbe	rs761117662
MSV3d	rs761117662
GWAS Ctlg	rs761117662

Max Magnitude

0

ClinVar
Risk	rs761117662(G;G) rs761117662(T;T)
Alt	rs761117662(G;G) rs761117662(T;T)
Reference	Rs761117662(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN5A
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.38647507C>T
CLNSRC
CLNACC	RCV000182966.2,