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 | 0.925 | 0.040 | 12 | 89619312 | intron variant | T/C;G | snv | 0.710 | 1.000 | 2 | 2013 | 2018 | |||||
|
66 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 0.710 | 1.000 | 2 | 2019 | 2019 | |||
|
1 | 18 | 6282594 | intron variant | A/C | snv | 0.27 | 0.710 | 1.000 | 1 | 2016 | 2016 | ||||||
|
7 | 0.827 | 0.080 | 16 | 1212024 | missense variant | A/G | snv | 7.0E-06 | 0.710 | 1.000 | 1 | 2016 | 2016 | ||||
|
1 | 5 | 132233934 | intron variant | T/C | snv | 0.59 | 0.710 | 1.000 | 1 | 2009 | 2009 | ||||||
|
19 | 0.882 | 0.160 | 12 | 119193787 | frameshift variant | TACTCAACATTTGG/- | del | 0.700 | 1.000 | 3 | 2016 | 2018 | |||||
|
5 | 19 | 11416089 | missense variant | T/A;C;G | snv | 0.700 | 1.000 | 2 | 2016 | 2016 | |||||||
|
4 | 4 | 80236549 | regulatory region variant | T/C | snv | 0.27 | 0.700 | 1.000 | 2 | 2015 | 2018 | ||||||
|
15 | 0.752 | 0.400 | 12 | 112477719 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 0.700 | 1.000 | 2 | 2001 | 2006 | |||
|
6 | 1.000 | 0.040 | 10 | 102856906 | intron variant | T/C | snv | 0.14 | 0.700 | 1.000 | 2 | 2015 | 2018 | ||||
|
4 | 7 | 27119517 | splice region variant | G/A;C | snv | 0.700 | 1.000 | 2 | 2016 | 2017 | |||||||
|
4 | 12 | 50144032 | missense variant | A/G;T | snv | 0.69 | 0.71 | 0.700 | 1.000 | 2 | 2016 | 2016 | |||||
|
9 | 0.925 | 0.120 | 1 | 10736809 | intron variant | T/C | snv | 0.32 | 0.700 | 1.000 | 2 | 2015 | 2018 | ||||
|
1 | 4 | 110409934 | intron variant | T/C | snv | 0.92 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 5 | 33204354 | intron variant | T/C | snv | 0.45 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
5 | 2 | 164155317 | intron variant | C/A;G | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 2 | 132431666 | intron variant | C/T | snv | 0.22 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||
|
3 | 8 | 55901862 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1 | 7 | 27288591 | intergenic variant | A/G | snv | 2.9E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 2 | 83065441 | intergenic variant | T/C | snv | 0.13 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||
|
1 | 2 | 83066256 | intergenic variant | C/T | snv | 0.13 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||
|
3 | 1 | 112646431 | intron variant | G/A | snv | 0.77 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
4 | 1 | 112501706 | intron variant | G/T | snv | 8.8E-02 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 12 | 45537190 | intron variant | C/A;G | snv | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
9 | 1.000 | 0.040 | 4 | 80259918 | intergenic variant | A/T | snv | 0.25 | 0.700 | 1.000 | 1 | 2018 | 2018 |