rs869025447

Orientation

minus

Stabilized

minus

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

Make rs869025447(-;C)

Make rs869025447(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

150958200

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs869025447
dbSNP (classic)	rs869025447
ClinGen	rs869025447
ebi	rs869025447
HLI	rs869025447
Exac	rs869025447
Gnomad	rs869025447
Varsome	rs869025447
LitVar	rs869025447
Map	rs869025447
PheGenI	rs869025447
Biobank	rs869025447
1000 genomes	rs869025447
hgdp	rs869025447
ensembl	rs869025447
geneview	rs869025447
scholar	rs869025447
google	rs869025447
pharmgkb	rs869025447
gwascentral	rs869025447
openSNP	rs869025447
23andMe	rs869025447
SNPshot	rs869025447
SNPdbe	rs869025447
MSV3d	rs869025447
GWAS Ctlg	rs869025447

Max Magnitude

0

ClinVar
Risk	rs869025447(C;C)
Alt	rs869025447(C;C)
Reference	Rs869025447(-;-)
Significance	Probable-Pathogenic
Disease	Long QT syndrome 2
Variation	info
Gene	KCNH2
CLNDBN	Long QT syndrome 2
Reversed	1
HGVS	NC_000007.13:g.150655289dupG
CLNSRC
CLNACC	RCV000208523.1,