rs1405999227, EGFR

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.
Progressive cGVHD
CUI: C3539781
Disease: Progressive cGVHD
40 0.925 0.160 7 55156637 missense variant A/G snv 4.0E-06 0.010 1.000 1 2018 2018
Progressive Neoplastic Disease
CUI: C0677932
Disease: Progressive Neoplastic Disease
40 0.925 0.160 7 55156637 missense variant A/G snv 4.0E-06 0.010 1.000 1 2018 2018
Xeroderma Pigmentosum, Complementation Group D
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
111 0.925 0.160 7 55156637 missense variant A/G snv 4.0E-06 0.010 1.000 1 2011 2011