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 | 12 | 100982873 | intron variant | A/G | snv | 4.6E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 11 | 107800953 | intron variant | A/G | snv | 0.14 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 12 | 109631385 | intergenic variant | G/T | snv | 1.2E-03 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
7 | 1 | 109928142 | intron variant | G/A | snv | 0.13 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 10 | 110871498 | non coding transcript exon variant | T/C | snv | 2.0E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 10 | 110996333 | intron variant | G/T | snv | 2.0E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
24 | 12 | 111280427 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
116 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||
|
1 | 10 | 11182702 | intron variant | T/C | snv | 0.15 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
5 | 0.925 | 0.120 | 12 | 112136812 | intron variant | C/T | snv | 5.9E-03 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
27 | 0.742 | 0.280 | 12 | 112379979 | intron variant | T/A | snv | 7.0E-03 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 9 | 114371911 | intron variant | C/T | snv | 0.43 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
4 | 3 | 120706484 | intron variant | T/C | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1 | 12 | 129167622 | intron variant | T/C | snv | 3.5E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 2 | 134842306 | intron variant | T/C | snv | 6.2E-02 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
6 | 1.000 | 0.080 | 6 | 135098493 | intron variant | A/G | snv | 0.24 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
1 | 6 | 136024992 | intron variant | C/T | snv | 3.2E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
6 | 4 | 145900258 | intron variant | C/A | snv | 0.15 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 3 | 157229738 | intron variant | A/G | snv | 1.7E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
3 | 2 | 169013785 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 10 | 17693720 | intron variant | T/C | snv | 3.4E-04 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 10 | 17833817 | synonymous variant | T/A | snv | 4.5E-04 | 0.49 | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||
|
1 | 10 | 17933413 | intergenic variant | T/C | snv | 0.25 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
2 | 4 | 181783398 | intergenic variant | A/G | snv | 0.18 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 10 | 18221519 | intron variant | G/A | snv | 0.62 | 0.700 | 1.000 | 1 | 2018 | 2018 |