rs104893875, SNCA

N. diseases: 13
Source: ALL
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.
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 0.010 1.000 1 2014 2014