rs199473141

Orientation

minus

Stabilized

minus

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

Make rs199473141(C;C)

Make rs199473141(C;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38598923

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473141
dbSNP (classic)	rs199473141
ClinGen	rs199473141
ebi	rs199473141
HLI	rs199473141
Exac	rs199473141
Gnomad	rs199473141
Varsome	rs199473141
LitVar	rs199473141
Map	rs199473141
PheGenI	rs199473141
Biobank	rs199473141
1000 genomes	rs199473141
hgdp	rs199473141
ensembl	rs199473141
geneview	rs199473141
scholar	rs199473141
google	rs199473141
pharmgkb	rs199473141
gwascentral	rs199473141
openSNP	rs199473141
23andMe	rs199473141
SNPshot	rs199473141
SNPdbe	rs199473141
MSV3d	rs199473141
GWAS Ctlg	rs199473141

Max Magnitude

0

ClinVar
Risk	rs199473141(C;C)
Alt	rs199473141(C;C)
Reference	Rs199473141(T;T)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000003.11:g.38640414A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058472.3,