rs863225288

Orientation

minus

Stabilized

minus

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

Make rs863225288(C;G)

Make rs863225288(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150951607

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs863225288
dbSNP (classic)	rs863225288
ClinGen	rs863225288
ebi	rs863225288
HLI	rs863225288
Exac	rs863225288
Gnomad	rs863225288
Varsome	rs863225288
LitVar	rs863225288
Map	rs863225288
PheGenI	rs863225288
Biobank	rs863225288
1000 genomes	rs863225288
hgdp	rs863225288
ensembl	rs863225288
geneview	rs863225288
scholar	rs863225288
google	rs863225288
pharmgkb	rs863225288
gwascentral	rs863225288
openSNP	rs863225288
23andMe	rs863225288
SNPshot	rs863225288
SNPdbe	rs863225288
MSV3d	rs863225288
GWAS Ctlg	rs863225288

Max Magnitude

0

ClinVar
Risk	rs863225288(G;G)
Alt	rs863225288(G;G)
Reference	Rs863225288(C;C)
Significance	Pathogenic
Disease	Long QT syndrome 2
Variation	info
Gene	KCNH2
CLNDBN	Long QT syndrome 2
Reversed	1
HGVS	NC_000007.13:g.150648695G>C
CLNSRC
CLNACC	RCV000202321.1,