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rs1060500670

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500670(-;-)
Make rs1060500670(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position150959642
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1060500670
dbSNP (old)rs1060500670
ClinGenrs1060500670
ebirs1060500670
HLIrs1060500670
Exacrs1060500670
Gnomadrs1060500670
Varsomers1060500670
Maprs1060500670
PheGenIrs1060500670
Biobankrs1060500670
1000 genomesrs1060500670
hgdprs1060500670
ensemblrs1060500670
gopubmedrs1060500670
geneviewrs1060500670
scholarrs1060500670
googlers1060500670
pharmgkbrs1060500670
gwascentralrs1060500670
openSNPrs1060500670
23andMers1060500670
23andMe allrs1060500670
SNPshotrs1060500670
SNPdbers1060500670
MSV3drs1060500670
GWAS Ctlgrs1060500670
Max Magnitude0
ClinVar
Risk rs1060500670(-;-)
Alt rs1060500670(-;-)
Reference Rs1060500670(G;G)
Significance Pathogenic
Disease Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150656730delC
CLNSRC
CLNACC RCV000477231.1,