rs1353702185, MDM2

N. diseases: 79
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.
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2006 2006
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2006 2006
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2006 2006
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1 2007 2007
Gastric Cardia Adenocarcinoma
CUI: C1333762
Disease: Gastric Cardia Adenocarcinoma
11 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2007 2007
Gastric Cardia Carcinoma
CUI: C1333763
Disease: Gastric Cardia Carcinoma
13 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2007 2007
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2007 2007
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2008 2008
Premenopausal breast cancer
CUI: C0741682
Disease: Premenopausal breast cancer
18 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2008 2008
Transitional cell carcinoma of bladder
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
158 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2008 2008
Treatment related acute myeloid leukaemia
CUI: C1336735
Disease: Treatment related acute myeloid leukaemia
4 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2008 2008
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.020 1.000 2 2009 2009
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Experimental Organism Basal Cell Carcinoma
CUI: C3811653
Disease: Experimental Organism Basal Cell Carcinoma
63 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Malignant neoplasm of skin
CUI: C0007114
Disease: Malignant neoplasm of skin
38 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009