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rs869025448

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025448(-;-)
Make rs869025448(-;C)
Make rs869025448(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position150952579
GeneKCNH2
is asnp
is mentioned by
dbSNPrs869025448
ebirs869025448
HLIrs869025448
Exacrs869025448
Varsomers869025448
Maprs869025448
PheGenIrs869025448
hapmaprs869025448
1000 genomesrs869025448
hgdprs869025448
ensemblrs869025448
gopubmedrs869025448
geneviewrs869025448
scholarrs869025448
googlers869025448
pharmgkbrs869025448
gwascentralrs869025448
openSNPrs869025448
23andMers869025448
23andMe allrs869025448
SNP Nexus

SNPshotrs869025448
SNPdbers869025448
MSV3drs869025448
GWAS Ctlgrs869025448
Max Magnitude0
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,