| 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. | ||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 2 | 45853263 | intron variant | T/C | snv | 0.35 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 11 | 88124996 | intron variant | T/A;C | snv | 1.3E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 7 | 155214802 | intron variant | G/A | snv | 0.59 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 2 | 212537150 | intron variant | C/G | snv | 1.7E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 22 | 50257071 | non coding transcript exon variant | G/A;C | snv | 2.0E-02; 4.0E-06 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 17 | 14390704 | intron variant | C/T | snv | 0.92 | 0.700 | 1.000 | 1 | 2008 | 2008 | ||||||
|
1 | 6 | 23856702 | non coding transcript exon variant | A/G | snv | 1.4E-05 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 1 | 22884066 | intron variant | C/T | snv | 8.2E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 9 | 136653172 | intron variant | C/T | snv | 0.21 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 15 | 86246747 | intron variant | G/T | snv | 0.13 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 19 | 52112198 | upstream gene variant | A/G | snv | 0.13 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 12 | 122901948 | TF binding site variant | T/C | snv | 2.4E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 |