rs786204839

Orientation

minus

Stabilized

minus

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

Make rs786204839(A;A)

Make rs786204839(A;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

38605949

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs786204839
dbSNP (classic)	rs786204839
ClinGen	rs786204839
ebi	rs786204839
HLI	rs786204839
Exac	rs786204839
Gnomad	rs786204839
Varsome	rs786204839
LitVar	rs786204839
Map	rs786204839
PheGenI	rs786204839
Biobank	rs786204839
1000 genomes	rs786204839
hgdp	rs786204839
ensembl	rs786204839
geneview	rs786204839
scholar	rs786204839
google	rs786204839
pharmgkb	rs786204839
gwascentral	rs786204839
openSNP	rs786204839
23andMe	rs786204839
SNPshot	rs786204839
SNPdbe	rs786204839
MSV3d	rs786204839
GWAS Ctlg	rs786204839

Max Magnitude

0

ClinVar
Risk	rs786204839(A;A)
Alt	rs786204839(A;A)
Reference	Rs786204839(T;T)
Significance	Pathogenic
Disease	not provided Cardiovascular phenotype Brugada syndrome
Variation	info
Gene	SCN5A
CLNDBN	not provided Cardiovascular phenotype Brugada syndrome
Reversed	1
HGVS	NC_000003.11:g.38647440A>T
CLNSRC
CLNACC	RCV000169744.3, RCV000241713.1, RCV000470912.1,