rs876660829, TP53

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.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 17 7673598 missense variant G/C;T snv 8.0E-06 0.010 1.000 1 1993 1993
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 17 7673598 missense variant G/C;T snv 8.0E-06 0.010 1.000 1 1993 1993