BOC, BOC cell adhesion associated, oncogene regulated, 91653
N. diseases: 33; N. variants: 7
Source: ALL
Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.776 | 0.080 | 3 | 113280713 | intron variant | G/A | snv | 2.7E-02 | 4.5E-02 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
0.776 | 0.080 | 3 | 113280713 | intron variant | G/A | snv | 2.7E-02 | 4.5E-02 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
0.776 | 0.080 | 3 | 113280713 | intron variant | G/A | snv | 2.7E-02 | 4.5E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 3 | 113280713 | intron variant | G/A | snv | 2.7E-02 | 4.5E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 3 | 113280713 | intron variant | G/A | snv | 2.7E-02 | 4.5E-02 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
0.776 | 0.080 | 3 | 113280713 | intron variant | G/A | snv | 2.7E-02 | 4.5E-02 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
0.776 | 0.080 | 3 | 113280713 | intron variant | G/A | snv | 2.7E-02 | 4.5E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 3 | 113280713 | intron variant | G/A | snv | 2.7E-02 | 4.5E-02 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
0.776 | 0.080 | 3 | 113280713 | intron variant | G/A | snv | 2.7E-02 | 4.5E-02 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
0.776 | 0.080 | 3 | 113280713 | intron variant | G/A | snv | 2.7E-02 | 4.5E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.080 | 3 | 113279940 | missense variant | G/A | snv | 3.2E-05 | 3.5E-05 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.700 | 0 | |||||||||
|
3 | 113272270 | non coding transcript exon variant | C/T | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.080 | 3 | 113272645 | synonymous variant | C/A;T | snv | 4.7E-04; 2.1E-02 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.925 | 0.040 | 3 | 113232682 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.925 | 0.040 | 3 | 113232682 | intron variant | C/A;T | snv |
|
Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
3 | 113255108 | intron variant | A/T | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
3 | 113239477 | intron variant | A/G | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |