rs781247868

Orientation

plus

Stabilized

plus

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

Make rs781247868(A;A)

Make rs781247868(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150974752

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs781247868
dbSNP (classic)	rs781247868
ClinGen	rs781247868
ebi	rs781247868
HLI	rs781247868
Exac	rs781247868
Gnomad	rs781247868
Varsome	rs781247868
LitVar	rs781247868
Map	rs781247868
PheGenI	rs781247868
Biobank	rs781247868
1000 genomes	rs781247868
hgdp	rs781247868
ensembl	rs781247868
geneview	rs781247868
scholar	rs781247868
google	rs781247868
pharmgkb	rs781247868
gwascentral	rs781247868
openSNP	rs781247868
23andMe	rs781247868
SNPshot	rs781247868
SNPdbe	rs781247868
MSV3d	rs781247868
GWAS Ctlg	rs781247868

Max Magnitude

0

ClinVar
Risk	rs781247868(A;A) rs781247868(C;C)
Alt	rs781247868(A;A) rs781247868(C;C)
Reference	Rs781247868(G;G)
Significance	Probable-Pathogenic
Disease	Cardiac arrhythmia
Variation	info
Gene	KCNH2
CLNDBN	Cardiac arrhythmia
Reversed	0
HGVS	NC_000007.13:g.150671840G>A
CLNSRC
CLNACC	RCV000181941.1,