rs794728417

Orientation

minus

Stabilized

minus

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

Make rs794728417(A;T)

Make rs794728417(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150974715

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs794728417
dbSNP (classic)	rs794728417
ClinGen	rs794728417
ebi	rs794728417
HLI	rs794728417
Exac	rs794728417
Gnomad	rs794728417
Varsome	rs794728417
LitVar	rs794728417
Map	rs794728417
PheGenI	rs794728417
Biobank	rs794728417
1000 genomes	rs794728417
hgdp	rs794728417
ensembl	rs794728417
geneview	rs794728417
scholar	rs794728417
google	rs794728417
pharmgkb	rs794728417
gwascentral	rs794728417
openSNP	rs794728417
23andMe	rs794728417
SNPshot	rs794728417
SNPdbe	rs794728417
MSV3d	rs794728417
GWAS Ctlg	rs794728417

Max Magnitude

0

ClinVar
Risk	rs794728417(T;T)
Alt	rs794728417(T;T)
Reference	Rs794728417(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150671803T>A
CLNSRC
CLNACC	RCV000181952.2,