rs7665116, PPARGC1A

N. diseases: 1
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.
Motor symptoms
CUI: C0426980
Disease: Motor symptoms
15 4 23851388 intron variant T/A;C snv 0.010 1 2012 2012