rs199473334

Orientation

minus

Stabilized

minus

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

Make rs199473334(A;A)

Make rs199473334(A;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38550443

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473334
dbSNP (classic)	rs199473334
ClinGen	rs199473334
ebi	rs199473334
HLI	rs199473334
Exac	rs199473334
Gnomad	rs199473334
Varsome	rs199473334
LitVar	rs199473334
Map	rs199473334
PheGenI	rs199473334
Biobank	rs199473334
1000 genomes	rs199473334
hgdp	rs199473334
ensembl	rs199473334
geneview	rs199473334
scholar	rs199473334
google	rs199473334
pharmgkb	rs199473334
gwascentral	rs199473334
openSNP	rs199473334
23andMe	rs199473334
SNPshot	rs199473334
SNPdbe	rs199473334
MSV3d	rs199473334
GWAS Ctlg	rs199473334

Max Magnitude

0

ClinVar
Risk	rs199473334(A;A)
Alt	rs199473334(A;A)
Reference	Rs199473334(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.38591934A>T
CLNSRC	ClinVar
CLNACC	RCV000058817.3,