rs370637245

Orientation

plus

Stabilized

plus

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

Make rs370637245(C;T)

Make rs370637245(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150952457

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs370637245
dbSNP (classic)	rs370637245
ClinGen	rs370637245
ebi	rs370637245
HLI	rs370637245
Exac	rs370637245
Gnomad	rs370637245
Varsome	rs370637245
LitVar	rs370637245
Map	rs370637245
PheGenI	rs370637245
Biobank	rs370637245
1000 genomes	rs370637245
hgdp	rs370637245
ensembl	rs370637245
geneview	rs370637245
scholar	rs370637245
google	rs370637245
pharmgkb	rs370637245
gwascentral	rs370637245
openSNP	rs370637245
23andMe	rs370637245
SNPshot	rs370637245
SNPdbe	rs370637245
MSV3d	rs370637245
GWAS Ctlg	rs370637245

Max Magnitude

0

ClinVar
Risk	rs370637245(T;T)
Alt	rs370637245(T;T)
Reference	Rs370637245(C;C)
Significance	Probable-Pathogenic
Disease	Cardiac arrhythmia
Variation	info
Gene	KCNH2
CLNDBN	Cardiac arrhythmia
Reversed	0
HGVS	NC_000007.13:g.150649545C>T
CLNSRC
CLNACC	RCV000181798.1,