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 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
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
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 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
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
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
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
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
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
Gastroesophageal reflux disease
CUI: C0017168
Disease: Gastroesophageal reflux disease
52 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2013 2013
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
Glioma
CUI: C0017638
Disease: Glioma
353 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2012 2012
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