rs199473064

Orientation

minus

Stabilized

minus

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

Make rs199473064(G;G)

Make rs199473064(G;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38620926

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473064
dbSNP (classic)	rs199473064
ClinGen	rs199473064
ebi	rs199473064
HLI	rs199473064
Exac	rs199473064
Gnomad	rs199473064
Varsome	rs199473064
LitVar	rs199473064
Map	rs199473064
PheGenI	rs199473064
Biobank	rs199473064
1000 genomes	rs199473064
hgdp	rs199473064
ensembl	rs199473064
geneview	rs199473064
scholar	rs199473064
google	rs199473064
pharmgkb	rs199473064
gwascentral	rs199473064
openSNP	rs199473064
23andMe	rs199473064
SNPshot	rs199473064
SNPdbe	rs199473064
MSV3d	rs199473064
GWAS Ctlg	rs199473064

Max Magnitude

0

ClinVar
Risk	rs199473064(G;G)
Alt	rs199473064(G;G)
Reference	Rs199473064(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.38662417A>C
CLNSRC	ClinVar
CLNACC	RCV000058761.3,