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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.040 | 10 | 100152437 | intron variant | C/T | snv | 0.32 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.160 | 2 | 100190052 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 0.040 | 16 | 10057377 | intron variant | G/A | snv | 8.2E-03 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.882 | 0.040 | 7 | 100689872 | intron variant | C/A;G | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.040 | 7 | 100699412 | regulatory region variant | G/C;T | snv |
|
0.700 | 1.000 | 2 | 2017 | 2019 | |||||||||
|
0.851 | 0.080 | 7 | 100701361 | upstream gene variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
0.882 | 0.040 | 7 | 100715797 | upstream gene variant | A/G | snv | 0.90 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 17 | 10080017 | intron variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 0.040 | 12 | 101060211 | intron variant | G/A | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 3 | 101082799 | intergenic variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 0.040 | 10 | 101719305 | intron variant | C/T | snv | 9.2E-02 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.040 | 8 | 10175915 | intron variant | A/T | snv | 0.28 |
|
0.700 | 1.000 | 3 | 2015 | 2019 | ||||||||
|
1.000 | 0.040 | 4 | 102191313 | intergenic variant | A/G | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 4 | 102225731 | intergenic variant | A/C | snv | 5.4E-02 |
|
0.700 | 1.000 | 2 | 2017 | 2019 | ||||||||
|
1.000 | 0.040 | 4 | 102225733 | intergenic variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 |
|
0.750 | 1.000 | 2 | 2015 | 2019 | ||||||||
|
0.925 | 0.040 | 5 | 102434022 | intron variant | C/T | snv | 0.64 |
|
0.810 | 0.667 | 2 | 2013 | 2016 | ||||||||
|
1.000 | 0.040 | 12 | 102492363 | intergenic variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.040 | 5 | 102523613 | regulatory region variant | C/T | snv | 0.66 |
|
0.800 | 1.000 | 2 | 2009 | 2011 | ||||||||
|
1.000 | 0.040 | 10 | 102540881 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
1.000 | 0.040 | 10 | 102664043 | downstream gene variant | T/G | snv | 0.13 |
|
0.700 | 1.000 | 2 | 2017 | 2019 | ||||||||
|
1.000 | 0.040 | 10 | 102696929 | intron variant | T/C | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 10 | 102852578 | intron variant | T/A | snv | 0.36 |
|
0.710 | 1.000 | 3 | 2014 | 2017 | ||||||||
|
1.000 | 0.040 | 10 | 102866129 | intron variant | G/A | snv | 0.36 |
|
0.700 | 1.000 | 2 | 2017 | 2019 | ||||||||
|
1.000 | 0.040 | 10 | 102869116 | intron variant | A/G | snv | 0.35 |
|
0.800 | 1.000 | 2 | 2013 | 2019 |