rs7684318, 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 1.000 0.040 4 89733852 intron variant T/C snv 0.19 0.730 1.000 1 2006 2012