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 | 11 | 134731013 | upstream gene variant | G/C;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1 | 1 | 201111046 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1 | 1 | 201373987 | non coding transcript exon variant | C/A;G;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1 | 16 | 20909796 | intron variant | A/G | snv | 8.6E-04 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 2 | 84884429 | intron variant | G/C | snv | 9.2E-04 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 4 | 185989889 | intergenic variant | G/A | snv | 1.0E-03 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 9 | 8457116 | intron variant | T/C | snv | 1.6E-03 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 12 | 55725460 | 3 prime UTR variant | A/G | snv | 2.7E-03 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 12 | 3460855 | intron variant | G/A | snv | 3.0E-03 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 1 | 169680550 | intron variant | T/C | snv | 3.0E-03 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 2 | 97982529 | intron variant | T/C | snv | 5.2E-03 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 7 | 4234812 | intron variant | G/A | snv | 1.6E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 13 | 81205735 | intergenic variant | G/A | snv | 3.2E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 12 | 89545547 | non coding transcript exon variant | G/A | snv | 3.5E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
5 | 0.851 | 0.040 | 1 | 201376359 | intron variant | G/A | snv | 0.27 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 11 | 131937277 | intron variant | A/G | snv | 0.33 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 8 | 70446868 | intergenic variant | C/G | snv | 0.41 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 8 | 70474669 | intron variant | T/A | snv | 0.47 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 8 | 70471122 | non coding transcript exon variant | T/C | snv | 0.49 | 0.700 | 1.000 | 1 | 2013 | 2013 |