Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.030 1.000 3 1997 2019
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.020 1.000 2 2010 2019
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.010 1.000 1 2007 2007
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		0.010 1.000 1 2004 2004
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma 		0.010 1.000 1 2004 2004
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		0.010 1.000 1 2004 2004
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.010 < 0.001 1 2007 2007
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2007 2007
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.010 1.000 1 2004 2004
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2019 2019
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0740457
Disease: Malignant neoplasm of kidney
Malignant neoplasm of kidney 		0.010 1.000 1 2007 2007
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 1995 1995
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2007 2007
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		0.010 1.000 1 2004 2004
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.010 1.000 1 2007 2007
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.010 1.000 1 1995 1995
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.010 1.000 1 2012 2012
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2007 2007
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C1167791
Disease: Skin toxicity
Skin toxicity 		0.010 1.000 1 2006 2006
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C1378703
Disease: Renal carcinoma
Renal carcinoma 		0.010 1.000 1 2007 2007
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
Childhood Non-Hodgkin Lymphoma 		0.010 1.000 1 2004 2004
dbSNP: rs1057520001
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		0.010 < 0.001 1 2007 2007