rs199473160

Orientation

minus

Stabilized

minus

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

Make rs199473160(C;C)

Make rs199473160(C;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38587413

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473160
dbSNP (classic)	rs199473160
ClinGen	rs199473160
ebi	rs199473160
HLI	rs199473160
Exac	rs199473160
Gnomad	rs199473160
Varsome	rs199473160
LitVar	rs199473160
Map	rs199473160
PheGenI	rs199473160
Biobank	rs199473160
1000 genomes	rs199473160
hgdp	rs199473160
ensembl	rs199473160
geneview	rs199473160
scholar	rs199473160
google	rs199473160
pharmgkb	rs199473160
gwascentral	rs199473160
openSNP	rs199473160
23andMe	rs199473160
SNPshot	rs199473160
SNPdbe	rs199473160
MSV3d	rs199473160
GWAS Ctlg	rs199473160

Max Magnitude

0

ClinVar
Risk	rs199473160(A;A) rs199473160(C;C)
Alt	rs199473160(A;A) rs199473160(C;C)
Reference	Rs199473160(G;G)
Significance	Untested
Disease	Congenital long QT syndrome Long QT syndrome
Variation	info
Gene	SCN5A
CLNDBN	Congenital long QT syndrome Long QT syndrome
Reversed	1
HGVS	NC_000003.11:g.38628904C>G; NC_000003.11:g.38628904C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058499.3, RCV000171699.1,