| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.724 | 0.160 | 10 | 8659256 | upstream gene variant | G/A | snv | 0.24 |
|
0.900 | 1.000 | 4 | 2008 | 2019 | ||||||||
|
0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 |
|
0.820 | 0.833 | 4 | 2014 | 2019 | ||||||||
|
0.763 | 0.480 | 7 | 140781617 | missense variant | C/A;G;T | snv |
|
0.800 | 1.000 | 4 | 2002 | 2014 | |||||||||
|
0.708 | 0.400 | 11 | 61785208 | non coding transcript exon variant | G/T | snv | 0.28 |
|
0.800 | 1.000 | 4 | 2014 | 2019 | ||||||||
|
0.790 | 0.080 | 20 | 7831703 | downstream gene variant | T/C | snv | 0.29 |
|
0.800 | 1.000 | 4 | 2013 | 2019 | ||||||||
|
0.776 | 0.080 | 12 | 4279105 | intron variant | C/T | snv | 8.7E-02 |
|
0.800 | 1.000 | 4 | 2013 | 2019 | ||||||||
|
0.790 | 0.080 | 11 | 74634505 | intron variant | T/G | snv | 0.40 |
|
0.810 | 1.000 | 4 | 2012 | 2019 | ||||||||
|
0.776 | 0.080 | 20 | 48723580 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 4 | 2015 | 2019 | |||||||||
|
0.925 | 0.160 | 2 | 47466663 | missense variant | G/T | snv |
|
0.700 | 1.000 | 4 | 1998 | 2005 | |||||||||
|
0.776 | 0.080 | 5 | 135163402 | intron variant | C/A | snv | 0.63 |
|
0.820 | 1.000 | 4 | 2013 | 2019 | ||||||||
|
0.732 | 0.240 | 20 | 6423634 | intergenic variant | C/A | snv | 0.34 |
|
0.860 | 1.000 | 4 | 2008 | 2019 | ||||||||
|
0.742 | 0.160 | 19 | 33041394 | intron variant | C/T | snv | 0.22 |
|
0.840 | 1.000 | 3 | 2008 | 2019 | ||||||||
|
0.776 | 0.080 | 17 | 10803924 | missense variant | G/A;C | snv |
|
0.700 | 1.000 | 3 | 2019 | 2019 | |||||||||
|
0.776 | 0.080 | 10 | 99591947 | intergenic variant | A/G | snv | 0.19 |
|
0.700 | 1.000 | 3 | 2015 | 2019 | ||||||||
|
0.716 | 0.160 | 10 | 112520943 | intron variant | T/C | snv | 0.13 |
|
0.720 | 1.000 | 3 | 2014 | 2019 | ||||||||
|
0.724 | 0.240 | 18 | 48927559 | intron variant | C/T | snv | 0.36 |
|
0.900 | 1.000 | 3 | 2007 | 2018 | ||||||||
|
0.776 | 0.080 | 15 | 32700910 | downstream gene variant | C/T | snv | 0.11 |
|
0.720 | 1.000 | 3 | 2011 | 2019 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.810 | 1.000 | 3 | 2014 | 2018 | ||||||||
|
0.790 | 0.080 | 20 | 62394395 | intron variant | C/T | snv | 0.22 |
|
0.800 | 1.000 | 3 | 2014 | 2019 | ||||||||
|
0.790 | 0.080 | 8 | 116611854 | intergenic variant | T/C | snv | 0.19 |
|
0.710 | 1.000 | 3 | 2016 | 2019 | ||||||||
|
0.689 | 0.400 | 5 | 1296371 | upstream gene variant | A/G | snv | 0.49 |
|
0.700 | 1.000 | 3 | 2019 | 2019 | ||||||||
|
0.701 | 0.240 | 14 | 53944201 | downstream gene variant | T/C | snv | 0.43 |
|
0.900 | 1.000 | 3 | 2008 | 2019 | ||||||||
|
0.776 | 0.080 | 20 | 6718948 | regulatory region variant | T/G | snv | 0.28 |
|
0.710 | 1.000 | 3 | 2011 | 2019 | ||||||||
|
0.790 | 0.080 | 8 | 116635549 | regulatory region variant | G/A;C | snv |
|
0.810 | 1.000 | 3 | 2014 | 2019 | |||||||||
|
0.790 | 0.080 | 15 | 32720301 | intron variant | A/G | snv | 0.25 |
|
0.800 | 1.000 | 3 | 2014 | 2019 |