Source: ALL
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: rs2737029
rs2737029
SNCA
1 1.000 0.040 4 89790619 intron variant T/C snv 0.45 0.720 1.000 4 2008 2018