rs2281983, PITX3

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.851 0.080 10 102231624 missense variant G/A;C;T snv 0.62; 8.3E-06 0.060 0.833 6 2011 2017
Dementia
CUI: C0497327
Disease: Dementia
176 0.851 0.080 10 102231624 missense variant G/A;C;T snv 0.62; 8.3E-06 0.010 1.000 1 2017 2017
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.851 0.080 10 102231624 missense variant G/A;C;T snv 0.62; 8.3E-06 0.010 1.000 1 2017 2017
Young onset Parkinson disease
CUI: C4275179
Disease: Young onset Parkinson disease
32 0.851 0.080 10 102231624 missense variant G/A;C;T snv 0.62; 8.3E-06 0.010 1.000 1 2011 2011