rs894278, SNCA

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 0.882 0.080 4 89813384 intron variant T/G snv 0.15 0.720 1.000 3 2009 2019