rs767521596

Orientation

plus

Stabilized

plus

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

Make rs767521596(-;-)

Make rs767521596(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150959591

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs767521596
dbSNP (classic)	rs767521596
ClinGen	rs767521596
ebi	rs767521596
HLI	rs767521596
Exac	rs767521596
Gnomad	rs767521596
Varsome	rs767521596
LitVar	rs767521596
Map	rs767521596
PheGenI	rs767521596
Biobank	rs767521596
1000 genomes	rs767521596
hgdp	rs767521596
ensembl	rs767521596
geneview	rs767521596
scholar	rs767521596
google	rs767521596
pharmgkb	rs767521596
gwascentral	rs767521596
openSNP	rs767521596
23andMe	rs767521596
SNPshot	rs767521596
SNPdbe	rs767521596
MSV3d	rs767521596
GWAS Ctlg	rs767521596

Max Magnitude

0

ClinVar
Risk	rs767521596(-;-)
Alt	rs767521596(-;-)
Reference	Rs767521596(G;G)
Significance	Pathogenic
Disease	not provided Long QT syndrome 2
Variation	info
Gene	KCNH2
CLNDBN	not provided Long QT syndrome 2
Reversed	0
HGVS	NC_000007.13:g.150656679delG
CLNSRC
CLNACC	RCV000181956.2, RCV000208221.1,