| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 |
|
0.900 | 1.000 | 3 | 2008 | 2018 | |||||||
|
0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv |
|
0.710 | 1.000 | 2 | 2013 | 2018 | |||||||||
|
0.827 | 0.120 | 1 | 24978623 | intergenic variant | T/C | snv | 0.55 |
|
0.700 | 1.000 | 2 | 2013 | 2016 | ||||||||
|
0.827 | 0.120 | 1 | 161502999 | upstream gene variant | C/A | snv | 0.65 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.827 | 0.120 | 1 | 67256884 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
1.000 | 0.040 | 1 | 24970693 | non coding transcript exon variant | G/A | snv | 0.44 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.827 | 0.120 | 1 | 113943285 | intron variant | T/C | snv | 8.1E-03 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.724 | 0.240 | 1 | 67203951 | intron variant | C/A;G | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
0.827 | 0.120 | 1 | 206788283 | intron variant | A/G | snv | 0.74 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.827 | 0.120 | 1 | 200909599 | intron variant | G/A | snv | 0.22 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.040 | 1 | 67281753 | downstream gene variant | G/A | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.040 | 1 | 210621464 | intron variant | T/C | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.807 | 0.200 | 1 | 160876494 | downstream gene variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.807 | 0.160 | 1 | 197732862 | intron variant | C/T | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.827 | 0.120 | 1 | 67237759 | intron variant | G/A | snv | 4.8E-03 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.724 | 0.240 | 1 | 81771892 | intron variant | C/T | snv | 0.71 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.827 | 0.120 | 1 | 2559766 | non coding transcript exon variant | C/T | snv | 4.1E-05; 0.55 | 0.58 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.925 | 0.080 | 1 | 200991179 | intron variant | G/A | snv | 0.27 | 0.27 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 |
|
0.710 | 1.000 | 1 | 2016 | 2017 | |||||||
|
0.827 | 0.120 | 1 | 200132792 | intron variant | A/G | snv | 0.84 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.776 | 0.280 | 1 | 206770623 | intron variant | C/A;T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.724 | 0.240 | 1 | 172869708 | intron variant | C/T | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.807 | 0.160 | 1 | 22373858 | intergenic variant | A/G | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.827 | 0.120 | 1 | 7962137 | intron variant | G/T | snv | 0.22 |
|
0.700 | 1.000 | 1 | 2016 | 2016 |