rs794728413

Orientation

minus

Stabilized

minus

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

Make rs794728413(G;T)

Make rs794728413(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150974743

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs794728413
dbSNP (classic)	rs794728413
ClinGen	rs794728413
ebi	rs794728413
HLI	rs794728413
Exac	rs794728413
Gnomad	rs794728413
Varsome	rs794728413
LitVar	rs794728413
Map	rs794728413
PheGenI	rs794728413
Biobank	rs794728413
1000 genomes	rs794728413
hgdp	rs794728413
ensembl	rs794728413
geneview	rs794728413
scholar	rs794728413
google	rs794728413
pharmgkb	rs794728413
gwascentral	rs794728413
openSNP	rs794728413
23andMe	rs794728413
SNPshot	rs794728413
SNPdbe	rs794728413
MSV3d	rs794728413
GWAS Ctlg	rs794728413

Max Magnitude

0

ClinVar
Risk	rs794728413(T;T)
Alt	rs794728413(T;T)
Reference	Rs794728413(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150671831C>A
CLNSRC
CLNACC	RCV000181943.2,