rs373394254

Orientation

plus

Stabilized

plus

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

Make rs373394254(A;A)

Make rs373394254(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150947386

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs373394254
dbSNP (classic)	rs373394254
ClinGen	rs373394254
ebi	rs373394254
HLI	rs373394254
Exac	rs373394254
Gnomad	rs373394254
Varsome	rs373394254
LitVar	rs373394254
Map	rs373394254
PheGenI	rs373394254
Biobank	rs373394254
1000 genomes	rs373394254
hgdp	rs373394254
ensembl	rs373394254
geneview	rs373394254
scholar	rs373394254
google	rs373394254
pharmgkb	rs373394254
gwascentral	rs373394254
openSNP	rs373394254
23andMe	rs373394254
SNPshot	rs373394254
SNPdbe	rs373394254
MSV3d	rs373394254
GWAS Ctlg	rs373394254

Max Magnitude

0

ClinVar
Risk	rs373394254(A;A)
Alt	rs373394254(A;A)
Reference	Rs373394254(G;G)
Significance	Probable-Pathogenic
Disease	Cardiac arrhythmia
Variation	info
Gene	KCNH2
CLNDBN	Cardiac arrhythmia
Reversed	0
HGVS	NC_000007.13:g.150644474G>A
CLNSRC
CLNACC	RCV000181909.1,