rs730881346, ATM

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.
Ataxia Telangiectasia
CUI: C0004135
Disease: Ataxia Telangiectasia
403 0.923 0.250 11 108257471 intron variant T/G snp 8.0E-06 3.2E-05 0.700 9 1998 2017
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
705 0.923 0.250 11 108257471 intron variant T/G snp 8.0E-06 3.2E-05 0.700 1 2015 2015
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
4866 0.923 0.250 11 108257471 intron variant T/G snp 8.0E-06 3.2E-05 0.700 1 2015 2015