rs2736990, SNCA

N. diseases: 2
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 89757390 intron variant G/A;T snv 0.860 1.000 6 2009 2018
Prion Diseases
CUI: C0162534
Disease: Prion Diseases
28 0.882 0.080 4 89757390 intron variant G/A;T snv 0.700 1.000 1 2012 2012