rs113488022, BRAF

N. diseases: 490
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.
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.876 89 2003 2019
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.988 83 2003 2020
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.986 74 2004 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.986 69 2002 2020
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.800 60 2004 2019
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.980 51 2005 2020
Hairy Cell Leukemia
CUI: C0023443
Disease: Hairy Cell Leukemia
4 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.979 48 2011 2019
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.909 44 2003 2019
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.907 43 2003 2019
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.927 41 2007 2018
Thyroid Nodule
CUI: C0040137
Disease: Thyroid Nodule
17 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.950 40 2006 2020
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.943 35 2004 2019
Anaplastic thyroid carcinoma
CUI: C0238461
Disease: Anaplastic thyroid carcinoma
16 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 1.000 34 2006 2019
Histiocytosis, Langerhans-Cell
CUI: C0019621
Disease: Histiocytosis, Langerhans-Cell
12 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.970 33 2012 2019
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.938 32 2004 2019
Secondary malignant neoplasm of colon and/or rectum
CUI: C4721579
Disease: Secondary malignant neoplasm of colon and/or rectum
68 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 1.000 28 2009 2019
Ganglioglioma
CUI: C0206716
Disease: Ganglioglioma
7 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.926 27 2011 2020
Childhood Pleomorphic Xanthoastrocytoma
CUI: C3899645
Disease: Childhood Pleomorphic Xanthoastrocytoma
7 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.958 24 2011 2020
Pleomorphic Xanthoastrocytoma
CUI: C0334586
Disease: Pleomorphic Xanthoastrocytoma
8 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.958 24 2011 2020
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 1.000 23 2003 2019
Hereditary Nonpolyposis Colorectal Cancer
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
1331 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.957 23 2004 2019
Melanocytic nevus
CUI: C0027962
Disease: Melanocytic nevus
33 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.955 22 2004 2019
Endocardial Cushion Defects
CUI: C0014116
Disease: Endocardial Cushion Defects
4 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 1.000 21 2012 2019
Split hand foot deformity 1
CUI: C2931019
Disease: Split hand foot deformity 1
8 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 1.000 21 2012 2019
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 1.000 20 2006 2019