rs199473055

Orientation

minus

Stabilized

minus

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

Make rs199473055(C;T)

Make rs199473055(T;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38630393

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473055
dbSNP (classic)	rs199473055
ClinGen	rs199473055
ebi	rs199473055
HLI	rs199473055
Exac	rs199473055
Gnomad	rs199473055
Varsome	rs199473055
LitVar	rs199473055
Map	rs199473055
PheGenI	rs199473055
Biobank	rs199473055
1000 genomes	rs199473055
hgdp	rs199473055
ensembl	rs199473055
geneview	rs199473055
scholar	rs199473055
google	rs199473055
pharmgkb	rs199473055
gwascentral	rs199473055
openSNP	rs199473055
23andMe	rs199473055
SNPshot	rs199473055
SNPdbe	rs199473055
MSV3d	rs199473055
GWAS Ctlg	rs199473055

Max Magnitude

0

ClinVar
Risk	rs199473055(G;G) rs199473055(T;T)
Alt	rs199473055(G;G) rs199473055(T;T)
Reference	Rs199473055(C;C)
Significance	Probable-Pathogenic
Disease	Brugada syndrome not provided Congenital long QT syndrome
Variation	info
Gene	SCN5A
CLNDBN	Brugada syndrome not provided Congenital long QT syndrome
Reversed	1
HGVS	NC_000003.11:g.38671884G>A; NC_000003.11:g.38671884G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058549.2, RCV000434418.1, RCV000058548.3,