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.
Adenocarcinoma Of Esophagus
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
81 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.020 0.500 2 2010 2013
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2013 2013
Adult Myelodysplastic Syndrome
CUI: C3900098
Disease: Adult Myelodysplastic Syndrome
20 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2012 2012
Blast Phase
CUI: C0005699
Disease: Blast Phase
14 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2014 2014
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
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
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
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2019 2019
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2015 2015
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2015 2015
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 Myelodysplastic Syndrome
CUI: C2347761
Disease: Childhood Myelodysplastic Syndrome
20 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2012 2012
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
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
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.020 0.500 2 2011 2015
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2013 2013
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
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.030 1.000 3 2010 2014
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2013 2013
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.020 1.000 2 2013 2014
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
63 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Familial Retinoblastoma
CUI: C0751483
Disease: Familial Retinoblastoma
4 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2011 2011
Febrile Neutropenia
CUI: C0746883
Disease: Febrile Neutropenia
14 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1 2012 2012