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.
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
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
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
Prostate Cancer, Hereditary, 7
CUI: C1853195
Disease: Prostate Cancer, Hereditary, 7
11 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1 2010 2010
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
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
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
Transient Ischemic Attack
CUI: C0007787
Disease: Transient Ischemic Attack
16 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2019 2019
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
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
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
Skin carcinoma
CUI: C0699893
Disease: Skin carcinoma
24 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2011 2011
Solid Neoplasm
CUI: C0280100
Disease: Solid Neoplasm
24 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2009 2009
Malignant neoplasm of soft tissue
CUI: C4551686
Disease: Malignant neoplasm of soft tissue
32 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.020 1.000 2 2012 2013
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
Sarcoma
CUI: C1261473
Disease: Sarcoma
42 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.020 1.000 2 2012 2013
Human papilloma virus infection
CUI: C0343641
Disease: Human papilloma virus infection
42 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2014 2014
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
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
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
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
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
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
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2013 2013
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