rs750949764, FOS

N. diseases: 2
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.
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 1.000 0.040 14 75280958 missense variant G/C snv 4.0E-06 0.010 1.000 1 2018 2018
Epithelioid hemangioendothelioma
CUI: C0206732
Disease: Epithelioid hemangioendothelioma
4 1.000 0.040 14 75280958 missense variant G/C snv 4.0E-06 0.010 1.000 1 2018 2018