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rs1060500623

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060500623(-;-)
Make rs1060500623(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position2445298
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs1060500623
dbSNP (old)rs1060500623
ClinGenrs1060500623
ebirs1060500623
HLIrs1060500623
Exacrs1060500623
Gnomadrs1060500623
Varsomers1060500623
Maprs1060500623
PheGenIrs1060500623
Biobankrs1060500623
1000 genomesrs1060500623
hgdprs1060500623
ensemblrs1060500623
gopubmedrs1060500623
geneviewrs1060500623
scholarrs1060500623
googlers1060500623
pharmgkbrs1060500623
gwascentralrs1060500623
openSNPrs1060500623
23andMers1060500623
23andMe allrs1060500623
SNPshotrs1060500623
SNPdbers1060500623
MSV3drs1060500623
GWAS Ctlgrs1060500623
Max Magnitude0
ClinVar
Risk rs1060500623(-;-)
Alt rs1060500623(-;-)
Reference Rs1060500623(C;C)
Significance Pathogenic
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2466528delC
CLNSRC
CLNACC RCV000458842.1,