rs763880032

Orientation

plus

Stabilized

plus

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

Make rs763880032(C;T)

Make rs763880032(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

38551187

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs763880032
dbSNP (classic)	rs763880032
ClinGen	rs763880032
ebi	rs763880032
HLI	rs763880032
Exac	rs763880032
Gnomad	rs763880032
Varsome	rs763880032
LitVar	rs763880032
Map	rs763880032
PheGenI	rs763880032
Biobank	rs763880032
1000 genomes	rs763880032
hgdp	rs763880032
ensembl	rs763880032
geneview	rs763880032
scholar	rs763880032
google	rs763880032
pharmgkb	rs763880032
gwascentral	rs763880032
openSNP	rs763880032
23andMe	rs763880032
SNPshot	rs763880032
SNPdbe	rs763880032
MSV3d	rs763880032
GWAS Ctlg	rs763880032

Max Magnitude

0

ClinVar
Risk	rs763880032(T;T)
Alt	rs763880032(T;T)
Reference	Rs763880032(C;C)
Significance	Probable-Pathogenic
Disease	not provided Brugada syndrome
Variation	info
Gene	SCN5A
CLNDBN	not provided Brugada syndrome
Reversed	0
HGVS	NC_000003.11:g.38592678C>T
CLNSRC
CLNACC	RCV000183107.1, RCV000462910.1,