rs794728423

Orientation

minus

Stabilized

minus

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

Make rs794728423(-;-)

Make rs794728423(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150958403

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728423
dbSNP (classic)	rs794728423
ClinGen	rs794728423
ebi	rs794728423
HLI	rs794728423
Exac	rs794728423
Gnomad	rs794728423
Varsome	rs794728423
LitVar	rs794728423
Map	rs794728423
PheGenI	rs794728423
Biobank	rs794728423
1000 genomes	rs794728423
hgdp	rs794728423
ensembl	rs794728423
geneview	rs794728423
scholar	rs794728423
google	rs794728423
pharmgkb	rs794728423
gwascentral	rs794728423
openSNP	rs794728423
23andMe	rs794728423
SNPshot	rs794728423
SNPdbe	rs794728423
MSV3d	rs794728423
GWAS Ctlg	rs794728423

Max Magnitude

0

ClinVar
Risk	rs794728423(-;-)
Alt	rs794728423(-;-)
Reference	Rs794728423(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150655491delG
CLNSRC
CLNACC	RCV000181961.2,