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rs1060499718

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs1060499718(-;-)
Make rs1060499718(-;GT)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2090418
GeneLOC105371049, MIR1225, PKD1
is asnp
is mentioned by
dbSNPrs1060499718
dbSNP (old)rs1060499718
ClinGenrs1060499718
ebirs1060499718
HLIrs1060499718
Exacrs1060499718
Gnomadrs1060499718
Varsomers1060499718
Maprs1060499718
PheGenIrs1060499718
Biobankrs1060499718
1000 genomesrs1060499718
hgdprs1060499718
ensemblrs1060499718
gopubmedrs1060499718
geneviewrs1060499718
scholarrs1060499718
googlers1060499718
pharmgkbrs1060499718
gwascentralrs1060499718
openSNPrs1060499718
23andMers1060499718
23andMe allrs1060499718
SNPshotrs1060499718
SNPdbers1060499718
MSV3drs1060499718
GWAS Ctlgrs1060499718
Max Magnitude0
ClinVar
Risk rs1060499718(-;-)
Alt rs1060499718(-;-)
Reference Rs1060499718(GT;GT)
Significance Pathogenic
Disease Polycystic kidney disease
Variation info
Gene PKD1 MIR1225 LOC105371049
CLNDBN Polycystic kidney disease, adult type
Reversed 1
HGVS NC_000016.9:g.2140419_2140420delAC
CLNSRC
CLNACC RCV000449570.1,