| 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 | 3 | 128075405 | intron variant | G/A | snv | 3.1E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 4 | 155725188 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
2 | 15 | 69390577 | intron variant | A/G | snv | 1.6E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 7 | 27532326 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1 | 7 | 1859811 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
3 | 1.000 | 0.040 | 7 | 7237584 | intron variant | C/G | snv | 1.0E-01 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 8 | 142916379 | intron variant | C/T | snv | 0.33 | 0.31 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 12 | 47860570 | intron variant | T/A | snv | 3.2E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 11 | 103527569 | intergenic variant | C/T | snv | 9.6E-02 | 0.700 | 1.000 | 1 | 2008 | 2008 | ||||||
|
1 | 2 | 61435420 | intron variant | C/A | snv | 0.32 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 19 | 18730347 | intron variant | C/A;G | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
6 | 1.000 | 0.040 | 1 | 62584148 | 3 prime UTR variant | G/A | snv | 0.36 | 0.700 | 1.000 | 1 | 2008 | 2008 | ||||
|
5 | 10 | 18439030 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1 | 15 | 41170270 | regulatory region variant | G/A | snv | 0.47 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 10 | 121240352 | intergenic variant | A/G | snv | 0.18 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 11 | 111793677 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
3 | 13 | 50532386 | intron variant | A/T | snv | 0.59 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
3 | 1.000 | 0.040 | 21 | 43339560 | intergenic variant | C/A;G;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 1 | 6616425 | intron variant | T/A;C;G | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
16 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
6 | 20 | 58589799 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||||
|
1 | 1 | 42041342 | non coding transcript exon variant | T/A;G | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
6 | 1.000 | 0.080 | 2 | 26691496 | upstream gene variant | C/T | snv | 0.48 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
12 | 0.807 | 0.240 | 5 | 75360714 | 3 prime UTR variant | T/C;G | snv | 0.37 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 16 | 292771 | non coding transcript exon variant | C/T | snv | 0.12 | 0.700 | 1.000 | 1 | 2019 | 2019 |