rs794728898

Orientation

minus

Stabilized

minus

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

Make rs794728898(A;G)

Make rs794728898(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

38550826

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs794728898
dbSNP (classic)	rs794728898
ClinGen	rs794728898
ebi	rs794728898
HLI	rs794728898
Exac	rs794728898
Gnomad	rs794728898
Varsome	rs794728898
LitVar	rs794728898
Map	rs794728898
PheGenI	rs794728898
Biobank	rs794728898
1000 genomes	rs794728898
hgdp	rs794728898
ensembl	rs794728898
geneview	rs794728898
scholar	rs794728898
google	rs794728898
pharmgkb	rs794728898
gwascentral	rs794728898
openSNP	rs794728898
23andMe	rs794728898
SNPshot	rs794728898
SNPdbe	rs794728898
MSV3d	rs794728898
GWAS Ctlg	rs794728898

Max Magnitude

0

ClinVar
Risk	rs794728898(G;G)
Alt	rs794728898(G;G)
Reference	Rs794728898(A;A)
Significance	Probable-Pathogenic
Disease	Brugada syndrome Cardiovascular phenotype
Variation	info
Gene	SCN5A
CLNDBN	Brugada syndrome Cardiovascular phenotype
Reversed	1
HGVS	NC_000003.11:g.38592317T>C
CLNSRC
CLNACC	RCV000227611.1, RCV000250980.1,