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.
Adult Diffuse Large B-Cell Lymphoma
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
46 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2012 2012
Adult Fibrosarcoma
CUI: C0278595
Disease: Adult Fibrosarcoma
9 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2003 2003
Adult Gliosarcoma
CUI: C1541317
Disease: Adult Gliosarcoma
5 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2020 2020
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2018 2018
Adult Malignant Peripheral Nerve Sheath Tumor
CUI: C0278622
Disease: Adult Malignant Peripheral Nerve Sheath Tumor
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2013 2013
Adult Medulloblastoma
CUI: C0278876
Disease: Adult Medulloblastoma
24 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2018 2018
ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED
CUI: C1845055
Disease: ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED
32 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2019 2019
Anaplastic ganglioglioma
CUI: C0431112
Disease: Anaplastic ganglioglioma
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2018 2018
Anaplastic Oligoastrocytoma
CUI: C0431108
Disease: Anaplastic Oligoastrocytoma
4 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2019 2019
Angiogenic Switch
CUI: C1510885
Disease: Angiogenic Switch
3 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
Angioimmunoblastic Lymphadenopathy
CUI: C0020981
Disease: Angioimmunoblastic Lymphadenopathy
8 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2015 2015
Arteriovenous hemangioma
CUI: C0334533
Disease: Arteriovenous hemangioma
14 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2020 2020
Arthralgia
CUI: C0003862
Disease: Arthralgia
27 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2012 2012
Astroblastoma
CUI: C0334587
Disease: Astroblastoma
4 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2019 2019
Atypical carcinoid tumor
CUI: C1266032
Disease: Atypical carcinoid tumor
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2018 2018
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1 2010 2010
Benign neurologic neoplasms
CUI: C0497550
Disease: Benign neurologic neoplasms
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2012 2012
Bile duct adenoma
CUI: C0008309
Disease: Bile duct adenoma
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2015 2015
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2015 2015
Cachexia
CUI: C0006625
Disease: Cachexia
11 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
Carcinoid tumor, malignant
CUI: C0391970
Disease: Carcinoid tumor, malignant
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2004 2004
Carcinoma ex pleomorphic adenoma
CUI: C0344460
Disease: Carcinoma ex pleomorphic adenoma
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2017 2017
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2015 2015
Carcinoma, Neuroendocrine
CUI: C0206695
Disease: Carcinoma, Neuroendocrine
7 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
Carcinoma, Signet Ring Cell
CUI: C0206696
Disease: Carcinoma, Signet Ring Cell
6 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2012 2012