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rs1060500661

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060500661(-;-)
Make rs1060500661(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position150951698
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1060500661
dbSNP (old)rs1060500661
ClinGenrs1060500661
ebirs1060500661
HLIrs1060500661
Exacrs1060500661
Gnomadrs1060500661
Varsomers1060500661
Maprs1060500661
PheGenIrs1060500661
Biobankrs1060500661
1000 genomesrs1060500661
hgdprs1060500661
ensemblrs1060500661
gopubmedrs1060500661
geneviewrs1060500661
scholarrs1060500661
googlers1060500661
pharmgkbrs1060500661
gwascentralrs1060500661
openSNPrs1060500661
23andMers1060500661
23andMe allrs1060500661
SNPshotrs1060500661
SNPdbers1060500661
MSV3drs1060500661
GWAS Ctlgrs1060500661
Max Magnitude0
ClinVar
Risk rs1060500661(-;-)
Alt rs1060500661(-;-)
Reference Rs1060500661(C;C)
Significance Pathogenic
Disease Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648786delG
CLNSRC
CLNACC RCV000470097.1,