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rs869025447

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025447(-;-)
Make rs869025447(-;C)
Make rs869025447(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position150958200
GeneKCNH2
is asnp
is mentioned by
dbSNPrs869025447
ebirs869025447
HLIrs869025447
Exacrs869025447
Varsomers869025447
Maprs869025447
PheGenIrs869025447
hapmaprs869025447
1000 genomesrs869025447
hgdprs869025447
ensemblrs869025447
gopubmedrs869025447
geneviewrs869025447
scholarrs869025447
googlers869025447
pharmgkbrs869025447
gwascentralrs869025447
openSNPrs869025447
23andMers869025447
23andMe allrs869025447
SNP Nexus

SNPshotrs869025447
SNPdbers869025447
MSV3drs869025447
GWAS Ctlgrs869025447
Max Magnitude0
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,