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rs1060499699

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499699(A;A)
Make rs1060499699(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2117579
GenePKD1
is asnp
is mentioned by
dbSNPrs1060499699
dbSNP (old)rs1060499699
ClinGenrs1060499699
ebirs1060499699
HLIrs1060499699
Exacrs1060499699
Gnomadrs1060499699
Varsomers1060499699
Maprs1060499699
PheGenIrs1060499699
Biobankrs1060499699
1000 genomesrs1060499699
hgdprs1060499699
ensemblrs1060499699
gopubmedrs1060499699
geneviewrs1060499699
scholarrs1060499699
googlers1060499699
pharmgkbrs1060499699
gwascentralrs1060499699
openSNPrs1060499699
23andMers1060499699
23andMe allrs1060499699
SNPshotrs1060499699
SNPdbers1060499699
MSV3drs1060499699
GWAS Ctlgrs1060499699
Max Magnitude0
ClinVar
Risk rs1060499699(A;A)
Alt rs1060499699(A;A)
Reference Rs1060499699(C;C)
Significance Probable-Pathogenic
Disease Polycystic kidney disease
Variation info
Gene PKD1
CLNDBN Polycystic kidney disease, adult type
Reversed 1
HGVS NC_000016.9:g.2167580G>T
CLNSRC
CLNACC RCV000449488.1,