rs794728366

Orientation

minus

Stabilized

minus

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

Make rs794728366(A;A)

Make rs794728366(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150952789

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728366
dbSNP (classic)	rs794728366
ClinGen	rs794728366
ebi	rs794728366
HLI	rs794728366
Exac	rs794728366
Gnomad	rs794728366
Varsome	rs794728366
LitVar	rs794728366
Map	rs794728366
PheGenI	rs794728366
Biobank	rs794728366
1000 genomes	rs794728366
hgdp	rs794728366
ensembl	rs794728366
geneview	rs794728366
scholar	rs794728366
google	rs794728366
pharmgkb	rs794728366
gwascentral	rs794728366
openSNP	rs794728366
23andMe	rs794728366
SNPshot	rs794728366
SNPdbe	rs794728366
MSV3d	rs794728366
GWAS Ctlg	rs794728366

Max Magnitude

0

ClinVar
Risk	rs794728366(A;A)
Alt	rs794728366(A;A)
Reference	Rs794728366(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150649877C>T
CLNSRC
CLNACC	RCV000181782.2,