rs794728392

Orientation

minus

Stabilized

minus

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

Make rs794728392(G;T)

Make rs794728392(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150950163

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728392
dbSNP (classic)	rs794728392
ClinGen	rs794728392
ebi	rs794728392
HLI	rs794728392
Exac	rs794728392
Gnomad	rs794728392
Varsome	rs794728392
LitVar	rs794728392
Map	rs794728392
PheGenI	rs794728392
Biobank	rs794728392
1000 genomes	rs794728392
hgdp	rs794728392
ensembl	rs794728392
geneview	rs794728392
scholar	rs794728392
google	rs794728392
pharmgkb	rs794728392
gwascentral	rs794728392
openSNP	rs794728392
23andMe	rs794728392
SNPshot	rs794728392
SNPdbe	rs794728392
MSV3d	rs794728392
GWAS Ctlg	rs794728392

Max Magnitude

0

ClinVar
Risk	rs794728392(T;T)
Alt	rs794728392(T;T)
Reference	Rs794728392(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150647251C>A
CLNSRC
CLNACC	RCV000181859.2,