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.
ASTROCYTOMA, LOW-GRADE, SOMATIC
CUI: C2674727
Disease: ASTROCYTOMA, LOW-GRADE, SOMATIC
1 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.700 0
Nongerminomatous Germ Cell Tumor
CUI: C1266158
Disease: Nongerminomatous Germ Cell Tumor
1 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.700 0
melanoma
CUI: C0025202
Disease: melanoma
515 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.800 0.979 477 2002 2020
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.990 98 2002 2020
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.986 69 2002 2020
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.790 0.970 33 2002 2019
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.800 1.000 30 2002 2019
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.750 1.000 16 2002 2018
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
154 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.800 1.000 15 2002 2019
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.750 1.000 12 2002 2015
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.800 0.947 475 2003 2020
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.800 0.959 387 2003 2019
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.876 89 2003 2019
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.988 83 2003 2020
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.909 44 2003 2019
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 0.907 43 2003 2019
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.800 1.000 26 2003 2020
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.100 1.000 23 2003 2019
Colonic Neoplasms
CUI: C0009375
Disease: Colonic Neoplasms
45 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.770 0.875 8 2003 2017
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.770 0.875 8 2003 2019
Follicular adenoma
CUI: C0205647
Disease: Follicular adenoma
5 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.060 1.000 6 2003 2018
Undifferentiated carcinoma
CUI: C0205698
Disease: Undifferentiated carcinoma
8 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.060 1.000 6 2003 2015
Thyroid Gland Follicular Adenoma
CUI: C0151468
Disease: Thyroid Gland Follicular Adenoma
14 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.030 1.000 3 2003 2018
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.020 0.500 2 2003 2015
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