rs864622174

Orientation

minus

Stabilized

minus

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

Make rs864622174(-;-)

Make rs864622174(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150947420

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs864622174
dbSNP (classic)	rs864622174
ClinGen	rs864622174
ebi	rs864622174
HLI	rs864622174
Exac	rs864622174
Gnomad	rs864622174
Varsome	rs864622174
LitVar	rs864622174
Map	rs864622174
PheGenI	rs864622174
Biobank	rs864622174
1000 genomes	rs864622174
hgdp	rs864622174
ensembl	rs864622174
geneview	rs864622174
scholar	rs864622174
google	rs864622174
pharmgkb	rs864622174
gwascentral	rs864622174
openSNP	rs864622174
23andMe	rs864622174
SNPshot	rs864622174
SNPdbe	rs864622174
MSV3d	rs864622174
GWAS Ctlg	rs864622174

Max Magnitude

0

ClinVar
Risk	rs864622174(-;-)
Alt	rs864622174(-;-)
Reference	Rs864622174(C;C)
Significance	Pathogenic
Disease	Long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150644508delG
CLNSRC
CLNACC	RCV000204955.1,