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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
10 | 0.790 | 0.080 | 19 | 21569009 | intron variant | G/C | snv | 0.23 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
10 | 0.776 | 0.080 | 20 | 7760329 | intergenic variant | A/G | snv | 0.13 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
17 | 0.708 | 0.280 | 1 | 210816167 | intron variant | T/G | snv | 0.21 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
10 | 0.790 | 0.080 | 16 | 78042662 | intron variant | A/C;G | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
17 | 0.708 | 0.280 | 12 | 49251457 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
10 | 0.776 | 0.080 | 12 | 50761880 | upstream gene variant | C/T | snv | 0.23 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
9 | 0.790 | 0.080 | 12 | 50823107 | downstream gene variant | T/C | snv | 0.42 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
10 | 0.776 | 0.080 | 10 | 99591947 | intergenic variant | A/G | snv | 0.19 | 0.700 | 1.000 | 3 | 2015 | 2019 | ||||
|
10 | 0.776 | 0.080 | 10 | 112962862 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
18 | 0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 | 0.700 | 1.000 | 4 | 2014 | 2019 | ||||
|
19 | 0.695 | 0.280 | 10 | 121575416 | intron variant | G/A;T | snv | 0.34 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
11 | 0.776 | 0.080 | 10 | 8697617 | intergenic variant | T/A | snv | 0.25 | 0.700 | 1.000 | 5 | 2014 | 2019 | ||||
|
9 | 0.790 | 0.080 | 3 | 134029945 | intron variant | T/C | snv | 0.23 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
9 | 0.790 | 0.080 | 3 | 155691561 | intron variant | G/A | snv | 1.8E-03 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
17 | 0.708 | 0.280 | 6 | 31347004 | intron variant | A/G | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
19 | 0.701 | 0.320 | 6 | 30374976 | intergenic variant | G/A | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
17 | 0.708 | 0.280 | 13 | 32394673 | intron variant | T/C | snv | 6.6E-03 | 6.0E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | |||
|
43 | 0.608 | 0.360 | 13 | 32398489 | stop gained | A/T | snv | 6.6E-03 | 6.0E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | |||
|
10 | 0.776 | 0.080 | 12 | 42740389 | intergenic variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
10 | 0.776 | 0.080 | 6 | 31042408 | regulatory region variant | T/C | snv | 2.2E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
10 | 0.790 | 0.080 | 2 | 97658891 | missense variant | G/A | snv | 7.0E-02 | 6.7E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||
|
10 | 0.776 | 0.080 | 8 | 116778675 | intron variant | C/A | snv | 3.0E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
14 | 0.776 | 0.080 | 4 | 144737912 | synonymous variant | T/C | snv | 6.6E-02 | 6.4E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||
|
17 | 0.708 | 0.280 | 14 | 68559662 | intron variant | G/A | snv | 0.23 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
11 | 0.763 | 0.080 | 18 | 48926786 | intron variant | A/T | snv | 0.50 | 0.700 | 1.000 | 2 | 2016 | 2019 |