rs104893877, SNCA

N. diseases: 59
Disease: Familial (FPAH) ×
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 0.614 0.360 4 89828149 missense variant C/T snv 0.100 1.000 13 2000 2018