rs1364898025, 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.
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.925 0.080 11 108227656 missense variant G/A snv 0.010 1.000 1 1998 1998
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.925 0.080 11 108227656 missense variant G/A snv 0.010 1.000 1 1998 1998
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.925 0.080 11 108227656 missense variant G/A snv 0.010 1.000 1 1998 1998