rs113388242, EIF4G1

N. diseases: 3
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 0.925 0.080 3 184327376 missense variant C/T snv 4.0E-05 7.0E-05 0.010 1.000 1 2011 2011
Lewy Body Disease
CUI: C0752347
Disease: Lewy Body Disease
41 0.925 0.080 3 184327376 missense variant C/T snv 4.0E-05 7.0E-05 0.010 1.000 1 2011 2011
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.925 0.080 3 184327376 missense variant C/T snv 4.0E-05 7.0E-05 0.010 1.000 1 2011 2011