rs121913377, BRAF

N. diseases: 480
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.
Childhood Pilocytic Astrocytoma
CUI: C1332995
Disease: Childhood Pilocytic Astrocytoma
10 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.800 10 2011 2020
Recurrent tumor
CUI: C0521158
Disease: Recurrent tumor
33 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.800 10 2010 2019
Pilocytic Astrocytoma
CUI: C0334583
Disease: Pilocytic Astrocytoma
14 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.842 19 2011 2020
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.857 14 2010 2019
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.070 0.857 7 2003 2019
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.875 88 2003 2019
Colonic Neoplasms
CUI: C0009375
Disease: Colonic Neoplasms
45 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.770 0.875 8 2003 2017
Nevus
CUI: C0027960
Disease: Nevus
43 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.080 0.875 8 2004 2017
Benign melanocytic nevus
CUI: C1456781
Disease: Benign melanocytic nevus
20 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.090 0.889 9 2004 2018
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.090 0.889 9 2003 2019
Carcinoma, Papillary
CUI: C0007133
Disease: Carcinoma, Papillary
9 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.900 10 2007 2018
Metastatic malignant neoplasm to brain
CUI: C0220650
Disease: Metastatic malignant neoplasm to brain
28 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.900 10 2012 2019
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.909 44 2003 2019
Adult Langerhans Cell Histiocytosis
CUI: C3900100
Disease: Adult Langerhans Cell Histiocytosis
2 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.917 12 2013 2019
Childhood Langerhans Cell Histiocytosis
CUI: C3899655
Disease: Childhood Langerhans Cell Histiocytosis
2 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.917 12 2013 2019
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.927 41 2007 2018
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.929 42 2003 2019
Ganglioglioma
CUI: C0206716
Disease: Ganglioglioma
7 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.929 28 2011 2020
Epithelioid glioblastoma
CUI: C4289580
Disease: Epithelioid glioblastoma
3 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.929 14 2014 2019
Lynch Syndrome
CUI: C4552100
Disease: Lynch Syndrome
65 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.929 14 2008 2019
Papillary Thyroid Microcarcinoma
CUI: C1709457
Disease: Papillary Thyroid Microcarcinoma
2 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.929 14 2005 2020
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.938 32 2004 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.943 35 2004 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.946 465 2003 2020
Thyroid Nodule
CUI: C0040137
Disease: Thyroid Nodule
17 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.947 38 2006 2020