rs2390669, STK39

N. diseases: 1
Source: GWASDB ×
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
224 1.000 0.040 2 168235432 intron variant A/C snv 0.14 0.700 1.000 1 2012 2012