rs199473155

Orientation

minus

Stabilized

minus

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

Make rs199473155(A;T)

Make rs199473155(T;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38587561

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473155
dbSNP (classic)	rs199473155
ClinGen	rs199473155
ebi	rs199473155
HLI	rs199473155
Exac	rs199473155
Gnomad	rs199473155
Varsome	rs199473155
LitVar	rs199473155
Map	rs199473155
PheGenI	rs199473155
Biobank	rs199473155
1000 genomes	rs199473155
hgdp	rs199473155
ensembl	rs199473155
geneview	rs199473155
scholar	rs199473155
google	rs199473155
pharmgkb	rs199473155
gwascentral	rs199473155
openSNP	rs199473155
23andMe	rs199473155
SNPshot	rs199473155
SNPdbe	rs199473155
MSV3d	rs199473155
GWAS Ctlg	rs199473155

Max Magnitude

0

ClinVar
Risk	rs199473155(G;G) rs199473155(T;T)
Alt	rs199473155(G;G) rs199473155(T;T)
Reference	Rs199473155(A;A)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000003.11:g.38629052T>A
CLNSRC	ClinVar
CLNACC	RCV000058493.3,