rs199473150

Orientation

minus

Stabilized

minus

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

Make rs199473150(C;T)

Make rs199473150(T;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38597799

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473150
dbSNP (classic)	rs199473150
ClinGen	rs199473150
ebi	rs199473150
HLI	rs199473150
Exac	rs199473150
Gnomad	rs199473150
Varsome	rs199473150
LitVar	rs199473150
Map	rs199473150
PheGenI	rs199473150
Biobank	rs199473150
1000 genomes	rs199473150
hgdp	rs199473150
ensembl	rs199473150
geneview	rs199473150
scholar	rs199473150
google	rs199473150
pharmgkb	rs199473150
gwascentral	rs199473150
openSNP	rs199473150
23andMe	rs199473150
SNPshot	rs199473150
SNPdbe	rs199473150
MSV3d	rs199473150
GWAS Ctlg	rs199473150

Max Magnitude

0

ClinVar
Risk	rs199473150(T;T)
Alt	rs199473150(T;T)
Reference	Rs199473150(C;C)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000003.11:g.38639290G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058485.3,