rs786203054, ATM

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.
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 1.000 0.200 11 108271074 missense variant T/A;G snv 0.700 1.000 5 1999 2017
Ataxia Telangiectasia
CUI: C0004135
Disease: Ataxia Telangiectasia
698 1.000 0.200 11 108271074 missense variant T/A;G snv 0.800 1.000 27 1995 2017