rs794728486

Orientation

minus

Stabilized

minus

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

Make rs794728486(A;A)

Make rs794728486(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150951450

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728486
dbSNP (classic)	rs794728486
ClinGen	rs794728486
ebi	rs794728486
HLI	rs794728486
Exac	rs794728486
Gnomad	rs794728486
Varsome	rs794728486
LitVar	rs794728486
Map	rs794728486
PheGenI	rs794728486
Biobank	rs794728486
1000 genomes	rs794728486
hgdp	rs794728486
ensembl	rs794728486
geneview	rs794728486
scholar	rs794728486
google	rs794728486
pharmgkb	rs794728486
gwascentral	rs794728486
openSNP	rs794728486
23andMe	rs794728486
SNPshot	rs794728486
SNPdbe	rs794728486
MSV3d	rs794728486
GWAS Ctlg	rs794728486

Max Magnitude

0

ClinVar
Risk	rs794728486(A;A)
Alt	rs794728486(A;A)
Reference	Rs794728486(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150648538C>T
CLNSRC
CLNACC	RCV000182037.2,