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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 |
|
0.900 | 0.917 | 2 | 2010 | 2016 | ||||||||
|
0.695 | 0.360 | 22 | 42130692 | missense variant | G/A | snv | 0.21 | 0.19 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.716 | 0.280 | 3 | 49534707 | 3 prime UTR variant | A/G | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.742 | 0.320 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 5.4E-02 | 5.9E-02 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.763 | 0.360 | 6 | 32945469 | intron variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.763 | 0.160 | 1 | 98037378 | intron variant | G/T | snv | 0.78 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.790 | 0.360 | 6 | 31504943 | intron variant | G/T | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.790 | 0.120 | 6 | 152469438 | intron variant | G/T | snv | 0.46 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.807 | 0.240 | 7 | 150339575 | intron variant | T/G | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.807 | 0.320 | 6 | 29978172 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
0.807 | 0.160 | 6 | 32707332 | upstream gene variant | T/C | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.827 | 0.040 | 3 | 52799203 | intron variant | G/A;C | snv |
|
0.820 | 1.000 | 2 | 2013 | 2019 | |||||||||
|
0.827 | 0.120 | 5 | 88367793 | intron variant | C/T | snv | 0.21 |
|
0.710 | 1.000 | 1 | 2016 | 2018 | ||||||||
|
0.827 | 0.040 | 10 | 60462349 | intron variant | T/C | snv | 8.0E-02 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.827 | 0.280 | 11 | 47255124 | intron variant | A/G | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.827 | 0.080 | 11 | 79366149 | intron variant | A/G | snv | 0.15 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.827 | 0.040 | 18 | 55084786 | intergenic variant | G/A | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.827 | 0.160 | 18 | 55539976 | intron variant | A/G | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.827 | 0.280 | 6 | 28986516 | intron variant | G/A | snv | 5.3E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.827 | 0.200 | 6 | 31979683 | non coding transcript exon variant | G/T | snv | 0.80 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.827 | 0.160 | 2 | 184668853 | intron variant | T/C | snv | 0.53 |
|
0.710 | 1.000 | 1 | 2017 | 2019 | ||||||||
|
0.851 | 0.040 | 18 | 55153893 | intergenic variant | A/G;T | snv |
|
0.700 | 1.000 | 2 | 2013 | 2019 | |||||||||
|
0.851 | 0.040 | 19 | 19948684 | intron variant | G/A | snv | 9.0E-02 |
|
0.700 | 1.000 | 1 | 2015 | 2015 |