rs794728374

Orientation

minus

Stabilized

minus

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

Make rs794728374(C;T)

Make rs794728374(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150951718

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728374
dbSNP (classic)	rs794728374
ClinGen	rs794728374
ebi	rs794728374
HLI	rs794728374
Exac	rs794728374
Gnomad	rs794728374
Varsome	rs794728374
LitVar	rs794728374
Map	rs794728374
PheGenI	rs794728374
Biobank	rs794728374
1000 genomes	rs794728374
hgdp	rs794728374
ensembl	rs794728374
geneview	rs794728374
scholar	rs794728374
google	rs794728374
pharmgkb	rs794728374
gwascentral	rs794728374
openSNP	rs794728374
23andMe	rs794728374
SNPshot	rs794728374
SNPdbe	rs794728374
MSV3d	rs794728374
GWAS Ctlg	rs794728374

Max Magnitude

0

ClinVar
Risk	rs794728374(T;T)
Alt	rs794728374(T;T)
Reference	Rs794728374(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150648806G>A
CLNSRC
CLNACC	RCV000181804.1,