rs760043106, TP53

N. diseases: 32
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.
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
206 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.700 1.000 6 2003 2016
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.020 1.000 2 2008 2009
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.710 1.000 2 2009 2016
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.020 1.000 2 2008 2009
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.710 1.000 2 2016 2016
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.020 1.000 2 2008 2009
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.010 1.000 1 2009 2009
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.010 1.000 1 2016 2016
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.010 1.000 1 2009 2009
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.010 1.000 1 2009 2009
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.010 1.000 1 2009 2009
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.010 1.000 1 2016 2016
Malignant neoplasm of gastrointestinal tract
CUI: C0685938
Disease: Malignant neoplasm of gastrointestinal tract
55 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.010 1.000 1 2008 2008
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.010 1.000 1 2009 2009
Mantle cell lymphoma
CUI: C4721414
Disease: Mantle cell lymphoma
19 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.010 1.000 1 2002 2002
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016