rs794728416

Orientation

minus

Stabilized

minus

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

Make rs794728416(C;T)

Make rs794728416(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150977883

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs794728416
dbSNP (classic)	rs794728416
ClinGen	rs794728416
ebi	rs794728416
HLI	rs794728416
Exac	rs794728416
Gnomad	rs794728416
Varsome	rs794728416
LitVar	rs794728416
Map	rs794728416
PheGenI	rs794728416
Biobank	rs794728416
1000 genomes	rs794728416
hgdp	rs794728416
ensembl	rs794728416
geneview	rs794728416
scholar	rs794728416
google	rs794728416
pharmgkb	rs794728416
gwascentral	rs794728416
openSNP	rs794728416
23andMe	rs794728416
SNPshot	rs794728416
SNPdbe	rs794728416
MSV3d	rs794728416
GWAS Ctlg	rs794728416

Max Magnitude

0

ClinVar
Risk	rs794728416(T;T)
Alt	rs794728416(T;T)
Reference	Rs794728416(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150674971G>A
CLNSRC
CLNACC	RCV000181951.2,