Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 6 | 139630553 | intron variant | A/G | snv | 0.58 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 19 | 35277334 | non coding transcript exon variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
4 | 9 | 4848297 | intron variant | A/G | snv | 0.19 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 1 | 230164735 | intron variant | C/G;T | snv | 0.56 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 4 | 68732288 | intergenic variant | A/T | snv | 0.19 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 10 | 94423594 | intron variant | T/C | snv | 0.51 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 11 | 5276199 | intron variant | G/A | snv | 0.33 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 11 | 65586679 | intron variant | G/A | snv | 0.45 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 14 | 73239461 | intron variant | T/G | snv | 8.1E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 8 | 97639920 | upstream gene variant | C/A | snv | 0.22 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 16 | 219907 | intron variant | A/G | snv | 0.21 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 10 | 24934438 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
2 | 15 | 78273478 | intron variant | C/T | snv | 8.5E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 1 | 205213744 | upstream gene variant | A/C | snv | 0.46 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 10 | 13715765 | intron variant | G/T | snv | 0.31 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 17 | 59877710 | intron variant | A/G | snv | 0.46 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 17 | 68432290 | intron variant | C/T | snv | 0.29 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 19 | 11182144 | intron variant | A/G | snv | 1.0E-01 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 22 | 31357863 | intergenic variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
2 | 22 | 50528205 | non coding transcript exon variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
3 | 6 | 30160096 | intron variant | C/T | snv | 0.11 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
3 | 22 | 21563570 | intron variant | A/C | snv | 0.17 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 6 | 3466533 | regulatory region variant | T/A | snv | 3.2E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 7 | 100628224 | splice region variant | C/T | snv | 3.1E-03 | 2.8E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
2 | 5 | 1085619 | intron variant | C/T | snv | 8.9E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 |