rs199473126

Orientation

minus

Stabilized

minus

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

Make rs199473126(G;T)

Make rs199473126(T;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38603890

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473126
dbSNP (classic)	rs199473126
ClinGen	rs199473126
ebi	rs199473126
HLI	rs199473126
Exac	rs199473126
Gnomad	rs199473126
Varsome	rs199473126
LitVar	rs199473126
Map	rs199473126
PheGenI	rs199473126
Biobank	rs199473126
1000 genomes	rs199473126
hgdp	rs199473126
ensembl	rs199473126
geneview	rs199473126
scholar	rs199473126
google	rs199473126
pharmgkb	rs199473126
gwascentral	rs199473126
openSNP	rs199473126
23andMe	rs199473126
SNPshot	rs199473126
SNPdbe	rs199473126
MSV3d	rs199473126
GWAS Ctlg	rs199473126

Max Magnitude

0

ClinVar
Risk	rs199473126(T;T)
Alt	rs199473126(T;T)
Reference	Rs199473126(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.38645381C>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058445.3, RCV000417257.1,