rs794728432

Orientation

minus

Stabilized

minus

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

Make rs794728432(-;C)

Make rs794728432(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150952849

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728432
dbSNP (classic)	rs794728432
ClinGen	rs794728432
ebi	rs794728432
HLI	rs794728432
Exac	rs794728432
Gnomad	rs794728432
Varsome	rs794728432
LitVar	rs794728432
Map	rs794728432
PheGenI	rs794728432
Biobank	rs794728432
1000 genomes	rs794728432
hgdp	rs794728432
ensembl	rs794728432
geneview	rs794728432
scholar	rs794728432
google	rs794728432
pharmgkb	rs794728432
gwascentral	rs794728432
openSNP	rs794728432
23andMe	rs794728432
SNPshot	rs794728432
SNPdbe	rs794728432
MSV3d	rs794728432
GWAS Ctlg	rs794728432

Max Magnitude

0

ClinVar
Risk	rs794728432(C;C)
Alt	rs794728432(C;C)
Reference	Rs794728432(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150649938dupG
CLNSRC
CLNACC	RCV000181970.2,