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.
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
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
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
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
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 1.000 1 2010 2010
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
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
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
206 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.020 1.000 2 2011 2016
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.020 1.000 2 2011 2015
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
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
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
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.020 0.500 2 2012 2015
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
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