rs1453167097, 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.
melanoma
CUI: C0025202
Disease: melanoma
515 0.925 0.080 17 7675172 missense variant A/C snv 0.010 1.000 1 2013 2013
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.925 0.080 17 7675172 missense variant A/C snv 0.010 1.000 1 2016 2016