rs730880374

Orientation

minus

Stabilized

minus

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

Make rs730880374(-;G)

Make rs730880374(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

150958132

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs730880374
dbSNP (classic)	rs730880374
ClinGen	rs730880374
ebi	rs730880374
HLI	rs730880374
Exac	rs730880374
Gnomad	rs730880374
Varsome	rs730880374
LitVar	rs730880374
Map	rs730880374
PheGenI	rs730880374
Biobank	rs730880374
1000 genomes	rs730880374
hgdp	rs730880374
ensembl	rs730880374
geneview	rs730880374
scholar	rs730880374
google	rs730880374
pharmgkb	rs730880374
gwascentral	rs730880374
openSNP	rs730880374
23andMe	rs730880374
SNPshot	rs730880374
SNPdbe	rs730880374
MSV3d	rs730880374
GWAS Ctlg	rs730880374

Max Magnitude

0

ClinVar
Risk	rs730880374(G;G)
Alt	rs730880374(G;G)
Reference	Rs730880374(-;-)
Significance	Probable-Pathogenic
Disease	Long QT syndrome 2
Variation	info
Gene	KCNH2
CLNDBN	Long QT syndrome 2
Reversed	1
HGVS	NC_000007.13:g.150655221dupC
CLNSRC
CLNACC	RCV000157260.1,