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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Acute lymphocytic leukemia
|
222 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.943 | 35 | 2001 | 2019 | ||||||
Breast Carcinoma
|
2793 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.813 | 32 | 2004 | 2019 | ||||||
Malignant neoplasm of breast
|
3417 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.813 | 32 | 2004 | 2019 | ||||||
Childhood Acute Lymphoblastic Leukemia
|
261 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.871 | 31 | 2005 | 2019 | ||||||
Colorectal Carcinoma
|
1962 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.806 | 31 | 2002 | 2019 | ||||||
Adult Acute Lymphocytic Leukemia
|
154 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.931 | 29 | 2002 | 2019 | ||||||
Malignant Neoplasms
|
1641 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 1.000 | 24 | 2002 | 2018 | ||||||
Malignant neoplasm of colon and/or rectum
|
502 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.870 | 23 | 2002 | 2018 | ||||||
Complete Trisomy 21 Syndrome
|
77 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.857 | 21 | 2003 | 2019 | ||||||
Down Syndrome
|
80 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.857 | 21 | 2003 | 2019 | ||||||
Hyperhomocysteinemia
|
45 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.762 | 21 | 2000 | 2018 | ||||||
Neural Tube Defects
|
122 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.667 | 21 | 1999 | 2019 | ||||||
Rheumatoid Arthritis
|
2387 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.905 | 21 | 2004 | 2018 | ||||||
Primary malignant neoplasm
|
1374 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 1.000 | 20 | 2002 | 2018 | ||||||
Coronary heart disease
|
1178 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.895 | 19 | 2001 | 2018 | ||||||
Schizophrenia
|
2897 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.684 | 19 | 2005 | 2020 | ||||||
Male infertility
|
146 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.688 | 16 | 2005 | 2019 | ||||||
Coronary Artery Disease
|
1577 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.800 | 15 | 2001 | 2020 | ||||||
Cardiovascular Diseases
|
711 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.917 | 12 | 2000 | 2019 | ||||||
Stomach Carcinoma
|
652 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.833 | 12 | 2005 | 2014 | ||||||
Diabetic Nephropathy
|
238 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 1.000 | 11 | 2000 | 2019 | ||||||
Ischemic stroke
|
704 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.909 | 11 | 2006 | 2018 | ||||||
Lymphoma, Non-Hodgkin
|
197 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 1.000 | 11 | 2003 | 2018 | ||||||
Malignant neoplasm of prostate
|
1082 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.727 | 11 | 2004 | 2016 | ||||||
Malignant neoplasm of stomach
|
615 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.100 | 0.818 | 11 | 2005 | 2014 |