rs6821591, PPARGC1A

N. diseases: 2
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 1.000 0.040 4 23795377 3 prime UTR variant C/T snv 0.53 0.020 1.000 2 2011 2018
Motor symptoms
CUI: C0426980
Disease: Motor symptoms
15 1.000 0.040 4 23795377 3 prime UTR variant C/T snv 0.53 0.010 1.000 1 2018 2018