rs199473555

Orientation

minus

Stabilized

minus

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

Make rs199473555(A;A)

Make rs199473555(A;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38630366

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473555
dbSNP (classic)	rs199473555
ClinGen	rs199473555
ebi	rs199473555
HLI	rs199473555
Exac	rs199473555
Gnomad	rs199473555
Varsome	rs199473555
LitVar	rs199473555
Map	rs199473555
PheGenI	rs199473555
Biobank	rs199473555
1000 genomes	rs199473555
hgdp	rs199473555
ensembl	rs199473555
geneview	rs199473555
scholar	rs199473555
google	rs199473555
pharmgkb	rs199473555
gwascentral	rs199473555
openSNP	rs199473555
23andMe	rs199473555
SNPshot	rs199473555
SNPdbe	rs199473555
MSV3d	rs199473555
GWAS Ctlg	rs199473555

Max Magnitude

0

ClinVar
Risk	rs199473555(A;A)
Alt	rs199473555(A;A)
Reference	Rs199473555(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000003.11:g.38671857C>T
CLNSRC	ClinVar
CLNACC	RCV000058568.3,