rs199472841

Orientation

minus

Stabilized

minus

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

Make rs199472841(G;T)

Make rs199472841(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150974868

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs199472841
dbSNP (classic)	rs199472841
ClinGen	rs199472841
ebi	rs199472841
HLI	rs199472841
Exac	rs199472841
Gnomad	rs199472841
Varsome	rs199472841
LitVar	rs199472841
Map	rs199472841
PheGenI	rs199472841
Biobank	rs199472841
1000 genomes	rs199472841
hgdp	rs199472841
ensembl	rs199472841
geneview	rs199472841
scholar	rs199472841
google	rs199472841
pharmgkb	rs199472841
gwascentral	rs199472841
openSNP	rs199472841
23andMe	rs199472841
SNPshot	rs199472841
SNPdbe	rs199472841
MSV3d	rs199472841
GWAS Ctlg	rs199472841

Max Magnitude

0

ClinVar
Risk	rs199472841(T;T)
Alt	rs199472841(T;T)
Reference	Rs199472841(G;G)
Significance	Untested
Disease	Short QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	short QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150671956C>A
CLNSRC	ClinVar
CLNACC	RCV000057920.3,