rs532891158

Orientation

plus

Stabilized

plus

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

Make rs532891158(C;G)

Make rs532891158(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150958107

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs532891158
dbSNP (classic)	rs532891158
ClinGen	rs532891158
ebi	rs532891158
HLI	rs532891158
Exac	rs532891158
Gnomad	rs532891158
Varsome	rs532891158
LitVar	rs532891158
Map	rs532891158
PheGenI	rs532891158
Biobank	rs532891158
1000 genomes	rs532891158
hgdp	rs532891158
ensembl	rs532891158
geneview	rs532891158
scholar	rs532891158
google	rs532891158
pharmgkb	rs532891158
gwascentral	rs532891158
openSNP	rs532891158
23andMe	rs532891158
SNPshot	rs532891158
SNPdbe	rs532891158
MSV3d	rs532891158
GWAS Ctlg	rs532891158

Max Magnitude

0

ClinVar
Risk	rs532891158(A;A) rs532891158(G;G) rs532891158(T;T)
Alt	rs532891158(A;A) rs532891158(G;G) rs532891158(T;T)
Reference	Rs532891158(C;C)
Significance	Probable-Pathogenic
Disease	Long QT syndrome not specified
Variation	info
Gene	KCNH2
CLNDBN	Long QT syndrome not specified
Reversed	0
HGVS	NC_000007.13:g.150655195C>A; NC_000007.13:g.150655195C>G
CLNSRC
CLNACC	RCV000297821.1, RCV000181769.3,