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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cutaneous lymphoma
|
3 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1 | 2006 | 2006 | |||||||
Epithelioid angiomyolipoma
|
3 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
Adult Acute Megakaryoblastic Leukemia
|
4 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2000 | 2000 | ||||||
Childhood Acute Megakaryoblastic Leukemia
|
4 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2000 | 2000 | ||||||
Familial Retinoblastoma
|
4 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
Treatment related acute myeloid leukaemia
|
4 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||||
Steroid Sulfatase Deficiency Disease
|
5 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||||
Indian childhood cirrhosis
|
6 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
Anaplasia
|
7 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
Skin Carcinogenesis
|
7 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||||
Mycosis Fungoides
|
8 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1 | 2006 | 2006 | |||||||
Squamous intraepithelial lesion
|
8 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
Undifferentiated carcinoma
|
8 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2003 | 2003 | ||||||
MYELOPROLIFERATIVE SYNDROME, TRANSIENT
|
9 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2000 | 2000 | ||||||
Ichthyosis, X-Linked
|
10 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||||
Keratosis
|
10 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||||
Extrapulmonary Small Cell Carcinoma
|
11 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
Gastric Cardia Adenocarcinoma
|
11 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
Prostate Cancer, Hereditary, 7
|
11 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1 | 2010 | 2010 | |||||||
SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT
|
12 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
Gastric Cardia Carcinoma
|
13 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
Infiltrating Cervical Carcinoma
|
13 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
Blast Phase
|
14 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
Febrile Neutropenia
|
14 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1 | 2012 | 2012 | |||||||
Fibroid Tumor
|
14 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.010 | 1.000 | 1 | 2019 | 2019 |