rs121913338, BRAF

N. diseases: 24
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.
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
79 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.800 1.000 1 2003 2003
melanoma
CUI: C0025202
Disease: melanoma
515 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.720 1.000 6 1986 2019
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.720 1.000 3 2016 2018
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.700 1.000 8 2002 2016
Adrenocortical carcinoma
CUI: C0206686
Disease: Adrenocortical carcinoma
46 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.700 1.000 1 2004 2004
Squamous cell carcinoma of the head and neck
348 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
158 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.020 1.000 2 2016 2017
Benign melanocytic nevus
CUI: C1456781
Disease: Benign melanocytic nevus
20 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.010 1.000 1 2004 2004
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.010 1.000 1 2017 2017
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.010 1.000 1 2012 2012
Histiocytic sarcoma
CUI: C0334663
Disease: Histiocytic sarcoma
8 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.010 1.000 1 2019 2019
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.010 1.000 1 2003 2003
Malignant neoplasm of colon and/or rectum
502 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.010 1.000 1 2016 2016
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.010 1.000 1 2015 2015
Melanocytic nevus
CUI: C0027962
Disease: Melanocytic nevus
33 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.010 1.000 1 2004 2004
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.010 1.000 1 2009 2009
Nevus
CUI: C0027960
Disease: Nevus
43 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.010 1.000 1 2004 2004
Papillary microcarcinoma
CUI: C1266051
Disease: Papillary microcarcinoma
3 0.677 0.400 7 140753354 missense variant T/A;C;G snv 0.010 1.000 1 2009 2009