rs794728875

Orientation

minus

Stabilized

minus

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

Make rs794728875(C;C)

Make rs794728875(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

38575334

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs794728875
dbSNP (classic)	rs794728875
ClinGen	rs794728875
ebi	rs794728875
HLI	rs794728875
Exac	rs794728875
Gnomad	rs794728875
Varsome	rs794728875
LitVar	rs794728875
Map	rs794728875
PheGenI	rs794728875
Biobank	rs794728875
1000 genomes	rs794728875
hgdp	rs794728875
ensembl	rs794728875
geneview	rs794728875
scholar	rs794728875
google	rs794728875
pharmgkb	rs794728875
gwascentral	rs794728875
openSNP	rs794728875
23andMe	rs794728875
SNPshot	rs794728875
SNPdbe	rs794728875
MSV3d	rs794728875
GWAS Ctlg	rs794728875

Max Magnitude

0

ClinVar
Risk	rs794728875(C;C)
Alt	rs794728875(C;C)
Reference	Rs794728875(T;T)
Significance	Probable-Pathogenic
Disease	not provided Brugada syndrome
Variation	info
Gene	SCN5A
CLNDBN	not provided Brugada syndrome
Reversed	1
HGVS	NC_000003.11:g.38616825A>G
CLNSRC
CLNACC	RCV000183040.2, RCV000476501.1,