Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3822086
rs3822086
SNCA
1 1.000 0.040 4 89743643 intron variant C/T snv 0.24 0.730 1.000 2 2011 2019