rs794728350

Orientation

minus

Stabilized

minus

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

Make rs794728350(C;G)

Make rs794728350(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150959703

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728350
dbSNP (classic)	rs794728350
ClinGen	rs794728350
ebi	rs794728350
HLI	rs794728350
Exac	rs794728350
Gnomad	rs794728350
Varsome	rs794728350
LitVar	rs794728350
Map	rs794728350
PheGenI	rs794728350
Biobank	rs794728350
1000 genomes	rs794728350
hgdp	rs794728350
ensembl	rs794728350
geneview	rs794728350
scholar	rs794728350
google	rs794728350
pharmgkb	rs794728350
gwascentral	rs794728350
openSNP	rs794728350
23andMe	rs794728350
SNPshot	rs794728350
SNPdbe	rs794728350
MSV3d	rs794728350
GWAS Ctlg	rs794728350

Max Magnitude

0

ClinVar
Risk	rs794728350(G;G)
Alt	rs794728350(G;G)
Reference	Rs794728350(C;C)
Significance	Pathogenic
Disease	Cardiac arrhythmia
Variation	info
Gene	KCNH2
CLNDBN	Cardiac arrhythmia
Reversed	1
HGVS	NC_000007.13:g.150656791G>C
CLNSRC
CLNACC	RCV000181751.1,