rs199473025

Orientation

minus

Stabilized

minus

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

Make rs199473025(C;T)

Make rs199473025(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150947347

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473025
dbSNP (classic)	rs199473025
ClinGen	rs199473025
ebi	rs199473025
HLI	rs199473025
Exac	rs199473025
Gnomad	rs199473025
Varsome	rs199473025
LitVar	rs199473025
Map	rs199473025
PheGenI	rs199473025
Biobank	rs199473025
1000 genomes	rs199473025
hgdp	rs199473025
ensembl	rs199473025
geneview	rs199473025
scholar	rs199473025
google	rs199473025
pharmgkb	rs199473025
gwascentral	rs199473025
openSNP	rs199473025
23andMe	rs199473025
SNPshot	rs199473025
SNPdbe	rs199473025
MSV3d	rs199473025
GWAS Ctlg	rs199473025

Max Magnitude

0

ClinVar
Risk	rs199473025(T;T)
Alt	rs199473025(T;T)
Reference	Rs199473025(C;C)
Significance	Probable-non-pathogenic
Disease	Congenital long QT syndrome Arrhythmogenic right ventricular cardiomyopathy Primary dilated cardiomyopathy Long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome Arrhythmogenic right ventricular cardiomyopathy Primary dilated cardiomyopathy Long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150644435G>A
CLNSRC	ClinVar
CLNACC	RCV000058201.3, RCV000143906.1, RCV000143907.1, RCV000157268.1,