rs869025448

Orientation

minus

Stabilized

minus

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

Make rs869025448(-;C)

Make rs869025448(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

150952579

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs869025448
dbSNP (classic)	rs869025448
ClinGen	rs869025448
ebi	rs869025448
HLI	rs869025448
Exac	rs869025448
Gnomad	rs869025448
Varsome	rs869025448
LitVar	rs869025448
Map	rs869025448
PheGenI	rs869025448
Biobank	rs869025448
1000 genomes	rs869025448
hgdp	rs869025448
ensembl	rs869025448
geneview	rs869025448
scholar	rs869025448
google	rs869025448
pharmgkb	rs869025448
gwascentral	rs869025448
openSNP	rs869025448
23andMe	rs869025448
SNPshot	rs869025448
SNPdbe	rs869025448
MSV3d	rs869025448
GWAS Ctlg	rs869025448

Max Magnitude

0

ClinVar
Risk	rs869025448(C;C)
Alt	rs869025448(C;C)
Reference	Rs869025448(-;-)
Significance	Probable-Pathogenic
Disease	Long QT syndrome 2
Variation	info
Gene	KCNH2
CLNDBN	Long QT syndrome 2
Reversed	1
HGVS	NC_000007.13:g.150649668dupG
CLNSRC
CLNACC	RCV000208164.1,