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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Conventional (Clear Cell) Renal Cell Carcinoma
|
222 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.010 | 1 | 2019 | 2019 | |||||
Exfoliation Syndrome
|
74 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.010 | 1 | 2018 | 2018 | |||||
Fanconi Anemia
|
173 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.010 | 1 | 2018 | 2018 | |||||
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
194 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.010 | 1 | 2018 | 2018 | |||||
FRIEDREICH ATAXIA 1
|
24 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.010 | 1 | 2018 | 2018 | |||||
Renal Cell Carcinoma
|
288 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.010 | 1 | 2019 | 2019 | |||||
Vitamin B 12 Deficiency
|
11 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.010 | 1 | 2018 | 2018 | |||||
Schizophrenia
|
2897 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.020 | 0.500 | 2 | 2010 | 2017 | ||||
Colorectal Carcinoma
|
1962 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.060 | 0.833 | 6 | 2008 | 2019 | ||||
Breast Carcinoma
|
2793 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.080 | 0.875 | 8 | 2009 | 2018 | ||||
Malignant neoplasm of breast
|
3417 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.080 | 0.875 | 8 | 2009 | 2018 | ||||
Acute lymphocytic leukemia
|
222 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.030 | 1.000 | 3 | 2013 | 2017 | ||||
Adult Acute Lymphocytic Leukemia
|
154 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.030 | 1.000 | 3 | 2013 | 2017 | ||||
Childhood Acute Lymphoblastic Leukemia
|
261 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.030 | 1.000 | 3 | 2013 | 2017 | ||||
Liver carcinoma
|
942 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.030 | 1.000 | 3 | 2018 | 2019 | ||||
Rheumatoid Arthritis
|
2387 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.030 | 1.000 | 3 | 2010 | 2014 | ||||
Adult Meningioma
|
30 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.020 | 1.000 | 2 | 2017 | 2017 | ||||
Alzheimer's Disease
|
1843 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.020 | 1.000 | 2 | 2012 | 2017 | ||||
Attention deficit hyperactivity disorder
|
420 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.020 | 1.000 | 2 | 2014 | 2018 | ||||
Carcinoma of lung
|
1204 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.020 | 1.000 | 2 | 2010 | 2012 | ||||
Coronary heart disease
|
1178 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.020 | 1.000 | 2 | 2015 | 2018 | ||||
Diabetes Mellitus, Non-Insulin-Dependent
|
2672 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.020 | 1.000 | 2 | 2014 | 2014 | ||||
Factor V Leiden mutation
|
46 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.020 | 1.000 | 2 | 2012 | 2016 | ||||
Hyperhomocysteinemia
|
45 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.020 | 1.000 | 2 | 2018 | 2018 | ||||
Hypertensive disease
|
1085 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.020 | 1.000 | 2 | 2014 | 2019 |