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rs863225288

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225288(C;G)
Make rs863225288(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951607
GeneKCNH2
is asnp
is mentioned by
dbSNPrs863225288
ebirs863225288
HLIrs863225288
Exacrs863225288
Varsomers863225288
Maprs863225288
PheGenIrs863225288
hapmaprs863225288
1000 genomesrs863225288
hgdprs863225288
ensemblrs863225288
gopubmedrs863225288
geneviewrs863225288
scholarrs863225288
googlers863225288
pharmgkbrs863225288
gwascentralrs863225288
openSNPrs863225288
23andMers863225288
23andMe allrs863225288
SNP Nexus

SNPshotrs863225288
SNPdbers863225288
MSV3drs863225288
GWAS Ctlgrs863225288
Max Magnitude0
ClinVar
Risk rs863225288(G;G)
Alt rs863225288(G;G)
Reference rs863225288(C;C)
Significance Pathogenic
Disease Long QT syndrome 2
Variation info
Gene KCNH2
CLNDBN Long QT syndrome 2
Reversed 1
HGVS NC_000007.13:g.150648695G>C
CLNSRC
CLNACC RCV000202321.1,