rs794728429

Orientation

minus

Stabilized

minus

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

Make rs794728429(-;-)

Make rs794728429(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150958090

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728429
dbSNP (classic)	rs794728429
ClinGen	rs794728429
ebi	rs794728429
HLI	rs794728429
Exac	rs794728429
Gnomad	rs794728429
Varsome	rs794728429
LitVar	rs794728429
Map	rs794728429
PheGenI	rs794728429
Biobank	rs794728429
1000 genomes	rs794728429
hgdp	rs794728429
ensembl	rs794728429
geneview	rs794728429
scholar	rs794728429
google	rs794728429
pharmgkb	rs794728429
gwascentral	rs794728429
openSNP	rs794728429
23andMe	rs794728429
SNPshot	rs794728429
SNPdbe	rs794728429
MSV3d	rs794728429
GWAS Ctlg	rs794728429

Max Magnitude

0

ClinVar
Risk	rs794728429(-;-)
Alt	rs794728429(-;-)
Reference	Rs794728429(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150655178delC
CLNSRC
CLNACC	RCV000181967.1,