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
|
515 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.800 | 0.981 | 464 | 2002 | 2020 | ||||||
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
|
1374 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.100 | 0.985 | 68 | 2002 | 2020 | ||||||
Neoplasms
|
1644 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.100 | 0.946 | 465 | 2003 | 2020 | ||||||
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
|
327 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.100 | 0.875 | 88 | 2003 | 2019 | ||||||
Thyroid Neoplasm
|
135 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.100 | 0.987 | 79 | 2003 | 2020 | ||||||
Secondary Neoplasm
|
85 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.100 | 0.909 | 44 | 2003 | 2019 | ||||||
Carcinogenesis
|
355 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.100 | 0.929 | 42 | 2003 | 2019 | ||||||
Cutaneous Melanoma
|
248 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.100 | 1.000 | 24 | 2003 | 2020 | ||||||
Carcinoma
|
103 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.100 | 1.000 | 21 | 2003 | 2019 | ||||||
Colorectal Neoplasms
|
609 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.090 | 0.889 | 9 | 2003 | 2019 | ||||||
Colonic Neoplasms
|
45 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.770 | 0.875 | 8 | 2003 | 2017 | ||||||
Multiple Myeloma
|
865 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.070 | 0.857 | 7 | 2003 | 2019 | ||||||
Follicular adenoma
|
5 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.060 | 1.000 | 6 | 2003 | 2018 | ||||||
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
|
14 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.030 | 1.000 | 3 | 2003 | 2018 | ||||||
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
|
9 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.010 | 1.000 | 1 | 2003 | 2003 | ||||||
Familial (FPAH)
|
276 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.010 | 1.000 | 1 | 2003 | 2003 | ||||||
Fibrosarcoma
|
9 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.010 | 1.000 | 1 | 2003 | 2003 | ||||||
Hereditary Melanoma
|
67 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.010 | 1 | 2003 | 2003 | |||||||
Nodular Goiter
|
12 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.010 | 1.000 | 1 | 2003 | 2003 | ||||||
Precancerous Conditions
|
18 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.010 | 1.000 | 1 | 2003 | 2003 | ||||||
Colorectal Carcinoma
|
1962 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.100 | 0.973 | 149 | 2004 | 2020 |