| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.614 | 0.520 | 9 | 22125504 | intron variant | G/C | snv | 0.41 |
|
0.900 | 0.944 | 2 | 2007 | 2019 | ||||||||
|
0.695 | 0.520 | 9 | 22098575 | intron variant | A/G;T | snv |
|
0.890 | 1.000 | 2 | 2007 | 2019 | |||||||||
|
0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 |
|
0.840 | 0.875 | 3 | 2013 | 2019 | ||||||||
|
0.851 | 0.160 | 9 | 22098620 | intron variant | A/G | snv | 0.40 |
|
0.820 | 1.000 | 3 | 2007 | 2018 | ||||||||
|
0.807 | 0.080 | 11 | 103789839 | intron variant | T/A;C | snv |
|
0.820 | 1.000 | 1 | 2012 | 2018 | |||||||||
|
0.882 | 0.120 | 15 | 90873320 | intron variant | C/A;G | snv |
|
0.810 | 1.000 | 2 | 2013 | 2018 | |||||||||
|
0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 |
|
0.810 | 1.000 | 2 | 2013 | 2018 | ||||||||
|
0.925 | 0.080 | 6 | 39207146 | intron variant | T/C | snv | 0.18 |
|
0.810 | 1.000 | 1 | 2013 | 2018 | ||||||||
|
0.827 | 0.120 | 9 | 22103814 | intron variant | A/G | snv | 0.63 |
|
0.810 | 1.000 | 1 | 2007 | 2018 | ||||||||
|
0.882 | 0.120 | 2 | 85582866 | upstream gene variant | C/T | snv | 0.52 |
|
0.810 | 1.000 | 1 | 2013 | 2018 | ||||||||
|
0.752 | 0.120 | 20 | 35176751 | missense variant | A/G | snv | 0.10 | 9.7E-02 |
|
0.810 | 1.000 | 1 | 2013 | 2018 | |||||||
|
1.000 | 0.040 | 2 | 19742712 | intergenic variant | G/A | snv | 0.11 |
|
0.800 | 1.000 | 4 | 2013 | 2018 | ||||||||
|
1.000 | 0.040 | 13 | 110165755 | intron variant | T/A | snv | 9.3E-02 |
|
0.800 | 1.000 | 2 | 2013 | 2018 | ||||||||
|
0.807 | 0.160 | 8 | 125478730 | intron variant | A/T | snv | 0.42 |
|
0.800 | 1.000 | 2 | 2013 | 2018 | ||||||||
|
0.882 | 0.080 | 4 | 147480038 | upstream gene variant | G/A;T | snv |
|
0.800 | 1.000 | 2 | 2013 | 2018 | |||||||||
|
0.882 | 0.080 | 17 | 17640408 | regulatory region variant | G/A | snv | 0.38 |
|
0.800 | 1.000 | 1 | 2013 | 2018 | ||||||||
|
1.000 | 0.040 | 10 | 44280862 | downstream gene variant | C/T | snv | 0.23 |
|
0.800 | 1.000 | 1 | 2007 | 2016 | ||||||||
|
0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 |
|
0.800 | 1.000 | 1 | 2014 | 2018 | ||||||||
|
1.000 | 0.040 | 2 | 145043894 | non coding transcript exon variant | T/C;G | snv | 0.58 |
|
0.800 | 1.000 | 1 | 2013 | 2018 | ||||||||
|
1.000 | 0.040 | 5 | 143137332 | intron variant | C/T | snv | 0.42 |
|
0.800 | 1.000 | 1 | 2013 | 2018 | ||||||||
|
0.882 | 0.080 | 8 | 19955669 | intron variant | G/A | snv | 0.14 |
|
0.800 | 1.000 | 1 | 2013 | 2018 | ||||||||
|
1.000 | 0.040 | 5 | 132331660 | intron variant | A/G | snv | 9.5E-02 |
|
0.800 | 1.000 | 1 | 2013 | 2018 | ||||||||
|
0.851 | 0.080 | 14 | 99667605 | intron variant | T/A;C | snv |
|
0.800 | 1.000 | 1 | 2013 | 2018 | |||||||||
|
0.851 | 0.080 | 1 | 154449591 | intron variant | T/C | snv | 0.60 |
|
0.800 | 1.000 | 1 | 2013 | 2018 | ||||||||
|
0.807 | 0.160 | 2 | 21063185 | intergenic variant | T/C | snv | 0.73 |
|
0.800 | 1.000 | 1 | 2013 | 2018 |