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.
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
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
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
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
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 0.956 367 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
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
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
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
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
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 1.000 21 2003 2019
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
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
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
Follicular adenoma
CUI: C0205647
Disease: Follicular adenoma
5 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.060 1.000 6 2003 2018
Undifferentiated carcinoma
CUI: C0205698
Disease: Undifferentiated carcinoma
8 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.060 1.000 6 2003 2015
Thyroid Gland Follicular Adenoma
CUI: C0151468
Disease: Thyroid Gland Follicular Adenoma
14 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.030 1.000 3 2003 2018
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.020 0.500 2 2003 2015
Adult Fibrosarcoma
CUI: C0278595
Disease: Adult Fibrosarcoma
9 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1.000 1 2003 2003
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1.000 1 2003 2003
Fibrosarcoma
CUI: C0016057
Disease: Fibrosarcoma
9 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1.000 1 2003 2003
Hereditary Melanoma
CUI: C1512419
Disease: Hereditary Melanoma
67 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1 2003 2003
Nodular Goiter
CUI: C0018023
Disease: Nodular Goiter
12 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1.000 1 2003 2003
Precancerous Conditions
CUI: C0032927
Disease: Precancerous Conditions
18 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1.000 1 2003 2003
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