rs563378859, TP53

N. diseases: 8
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 0.851 0.320 17 7675146 missense variant G/A snv 4.0E-06 2.1E-05 0.030 1.000 3 2008 2016
Apraxia, Developmental Verbal
CUI: C0750927
Disease: Apraxia, Developmental Verbal
21 0.851 0.320 17 7675146 missense variant G/A snv 4.0E-06 2.1E-05 0.010 1.000 1 2015 2015
Hereditary Melanoma
CUI: C1512419
Disease: Hereditary Melanoma
67 0.851 0.320 17 7675146 missense variant G/A snv 4.0E-06 2.1E-05 0.010 1.000 1 2001 2001
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.851 0.320 17 7675146 missense variant G/A snv 4.0E-06 2.1E-05 0.010 1.000 1 2012 2012
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.851 0.320 17 7675146 missense variant G/A snv 4.0E-06 2.1E-05 0.010 1.000 1 2010 2010
Mantle cell lymphoma
CUI: C4721414
Disease: Mantle cell lymphoma
19 0.851 0.320 17 7675146 missense variant G/A snv 4.0E-06 2.1E-05 0.010 1.000 1 2012 2012
Multiple tumors
CUI: C0260037
Disease: Multiple tumors
12 0.851 0.320 17 7675146 missense variant G/A snv 4.0E-06 2.1E-05 0.010 1.000 1 2001 2001
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.851 0.320 17 7675146 missense variant G/A snv 4.0E-06 2.1E-05 0.010 1.000 1 2010 2010