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.
Anaplastic thyroid carcinoma
CUI: C0238461
Disease: Anaplastic thyroid carcinoma
16 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 1.000 34 2006 2019
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 1.000 20 2006 2019
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
Hyperplastic Polyp
CUI: C0333983
Disease: Hyperplastic Polyp
22 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.090 1.000 9 2006 2016
Melanocytic nevus of skin
CUI: C3665593
Disease: Melanocytic nevus of skin
3 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.080 1.000 8 2006 2019
Follicular thyroid carcinoma
CUI: C0206682
Disease: Follicular thyroid carcinoma
28 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.060 1.000 6 2006 2018
Anaplasia
CUI: C0002793
Disease: Anaplasia
7 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.050 1.000 5 2006 2016
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.050 1.000 5 2006 2018
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.050 1.000 5 2006 2018
Progressive cGVHD
CUI: C3539781
Disease: Progressive cGVHD
40 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.050 1.000 5 2006 2018
Progressive Neoplastic Disease
CUI: C0677932
Disease: Progressive Neoplastic Disease
40 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.050 1.000 5 2006 2018
Secondary malignant neoplasm of lung
CUI: C0153676
Disease: Secondary malignant neoplasm of lung
20 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.050 1.000 5 2006 2015
Follicular Variant Thyroid Gland Papillary Carcinoma
CUI: C3714651
Disease: Follicular Variant Thyroid Gland Papillary Carcinoma
13 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.030 0.667 3 2006 2018
Human immunodeficiency virus (HIV) II infection category B1
CUI: C3854222
Disease: Human immunodeficiency virus (HIV) II infection category B1
56 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1.000 1 2006 2006
Malignant melanoma of choroid
CUI: C0346388
Disease: Malignant melanoma of choroid
5 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1.000 1 2006 2006
Merkel cell carcinoma
CUI: C0007129
Disease: Merkel cell carcinoma
10 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1 2006 2006
premalignant lesion
CUI: C0850639
Disease: premalignant lesion
5 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1.000 1 2006 2006
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
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
Turcot syndrome (disorder)
CUI: C0265325
Disease: Turcot syndrome (disorder)
75 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.070 1.000 7 2007 2019
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.060 1.000 6 2007 2015
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.050 1.000 5 2007 2015
MSI-high
CUI: C4523846
Disease: MSI-high
9 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.030 1.000 3 2007 2015
Carcinoma, Endometrioid
CUI: C0206687
Disease: Carcinoma, Endometrioid
12 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.020 1.000 2 2007 2013
Serous cystadenoma, borderline malignancy
CUI: C0334355
Disease: Serous cystadenoma, borderline malignancy
2 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.020 1.000 2 2007 2018