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.
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.100 0.900 10 2006 2017
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
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.100 0.733 15 2007 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.100 0.733 15 2007 2017
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.050 1.000 5 2007 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.040 1.000 4 2007 2019
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.020 0.500 2 2007 2011
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.020 0.500 2 2007 2011
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
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.050 0.800 5 2008 2017
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.030 1.000 3 2008 2014
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
melanoma
CUI: C0025202
Disease: melanoma
515 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.050 1.000 5 2009 2014
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