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
|
1644 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.100 | 0.947 | 19 | 2005 | 2019 | ||||||
Colorectal Neoplasms
|
609 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 16 | 2005 | 2015 | ||||||
Colorectal Carcinoma
|
1962 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.100 | 1.000 | 10 | 2004 | 2019 | ||||||
Secondary malignant neoplasm of colon and/or rectum
|
68 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.090 | 0.889 | 9 | 2010 | 2017 | ||||||
Leukemia, Myelocytic, Acute
|
6892 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 5 | 1987 | 2012 | ||||||
Malignant tumor of colon
|
688 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.050 | 1.000 | 5 | 2006 | 2019 | ||||||
Colon Carcinoma
|
275 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.040 | 1.000 | 4 | 2015 | 2019 | ||||||
Malignant neoplasm of colon and/or rectum
|
502 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.040 | 1.000 | 4 | 2014 | 2019 | ||||||
Thyroid Neoplasm
|
135 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 4 | 2007 | 2013 | ||||||
Non-Small Cell Lung Carcinoma
|
712 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 3 | 2002 | 2008 | ||||||
Adenocarcinoma
|
168 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.020 | 1.000 | 2 | 2016 | 2016 | ||||||
Neoplasm Metastasis
|
327 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.020 | 1.000 | 2 | 2009 | 2020 | ||||||
ovarian neoplasm
|
757 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 2 | 2008 | 2011 | ||||||
APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS
|
5 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||
Autoimmune Lymphoproliferative Syndrome
|
22 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
Hematologic Neoplasms
|
60 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
Hypoglycemia
|
42 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||||
Juvenile Myelomonocytic Leukemia
|
70 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.810 | 1.000 | 1 | 2015 | 2015 | ||||||
Lymphoma, Follicular
|
83 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
Lymphoma, T-Cell, Cutaneous
|
5 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
Malignant Neoplasms
|
1641 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
melanoma
|
515 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
Mycosis Fungoides
|
8 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
Refractory Colorectal Carcinoma
|
2 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
Secondary Neoplasm
|
85 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2009 | 2009 |