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.
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
melanoma
CUI: C0025202
Disease: melanoma
515 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.800 0.981 464 2002 2020
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.973 149 2004 2020
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.989 95 2002 2020
Metastatic melanoma
CUI: C0278883
Disease: Metastatic melanoma
42 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 1.000 91 2004 2020
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.987 79 2003 2020
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.985 68 2002 2020
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.980 51 2005 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
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
Childhood Pleomorphic Xanthoastrocytoma
CUI: C3899645
Disease: Childhood Pleomorphic Xanthoastrocytoma
7 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.958 24 2011 2020
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 1.000 24 2003 2020
Pleomorphic Xanthoastrocytoma
CUI: C0334586
Disease: Pleomorphic Xanthoastrocytoma
8 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.958 24 2011 2020
Glioma
CUI: C0017638
Disease: Glioma
353 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 1.000 19 2011 2020
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
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
Childhood Ganglioglioma
CUI: C1332969
Disease: Childhood Ganglioglioma
4 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 1.000 13 2011 2020
Adult Pilocytic Astrocytoma
CUI: C0280781
Disease: Adult Pilocytic Astrocytoma
10 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.800 10 2011 2020
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
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 1.000 10 2006 2020
Low grade glioma
CUI: C1997217
Disease: Low grade glioma
10 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.030 1.000 3 2017 2020
recurrent papillary thyroid cancer
CUI: C4733538
Disease: recurrent papillary thyroid cancer
2 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.020 1.000 2 2011 2020
Adult Gliosarcoma
CUI: C1541317
Disease: Adult Gliosarcoma
5 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1.000 1 2020 2020
Arteriovenous hemangioma
CUI: C0334533
Disease: Arteriovenous hemangioma
14 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1.000 1 2020 2020
Childhood Gliosarcoma
CUI: C3899658
Disease: Childhood Gliosarcoma
5 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1.000 1 2020 2020