rs946880677, FAP

N. diseases: 4
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.
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.882 0.080 2 162224488 missense variant T/C snv 0.010 1.000 1 2005 2005
CNS disorder
CUI: C0007682
Disease: CNS disorder
11 0.882 0.080 2 162224488 missense variant T/C snv 0.010 1.000 1 2005 2005
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.882 0.080 2 162224488 missense variant T/C snv 0.010 1.000 1 2005 2005
Polyneuropathy
CUI: C0152025
Disease: Polyneuropathy
32 0.882 0.080 2 162224488 missense variant T/C snv 0.010 1.000 1 2005 2005