Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
4 | 0.851 | 0.080 | 10 | 102238914 | intron variant | A/T | snv | 0.66 | 0.010 | < 0.001 | 1 | 2017 | 2017 | ||||
|
7 | 0.851 | 0.160 | 6 | 162262672 | missense variant | T/C;G | snv | 0.010 | < 0.001 | 1 | 2007 | 2007 | |||||
|
4 | 0.851 | 0.040 | 7 | 56104344 | missense variant | G/A | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||
|
3 | 0.882 | 0.080 | 16 | 4510300 | 3 prime UTR variant | G/A | snv | 0.54 | 0.020 | 0.500 | 2 | 2015 | 2017 | ||||
|
3 | 0.882 | 0.040 | 12 | 40283897 | missense variant | C/T | snv | 7.4E-04 | 2.2E-04 | 0.020 | 0.500 | 2 | 2007 | 2018 | |||
|
3 | 0.882 | 0.240 | 5 | 161854239 | synonymous variant | T/C | snv | 0.26 | 0.24 | 0.010 | 1.000 | 1 | 2006 | 2006 | |||
|
4 | 0.882 | 0.080 | 3 | 38925454 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 0.010 | 1.000 | 1 | 2017 | 2017 | |||
|
3 | 0.882 | 0.080 | 16 | 4476291 | 5 prime UTR variant | A/G | snv | 0.74 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
3 | 0.882 | 0.040 | 16 | 31185061 | missense variant | C/G;T | snv | 1.3E-04; 4.1E-06 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
3 | 0.882 | 0.080 | 16 | 89919458 | missense variant | G/A | snv | 9.6E-04 | 2.7E-04 | 0.010 | 1.000 | 1 | 2018 | 2018 | |||
|
3 | 0.882 | 0.040 | 10 | 102244438 | upstream gene variant | G/A | snv | 0.14 | 0.010 | < 0.001 | 1 | 2017 | 2017 | ||||
|
3 | 0.882 | 0.080 | 9 | 28717575 | intergenic variant | T/C;G | snv | 0.35 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
2 | 0.925 | 0.040 | 16 | 31189158 | stop gained | C/T | snv | 0.050 | 1.000 | 5 | 2013 | 2016 | |||||
|
2 | 0.925 | 0.040 | 9 | 28294233 | intron variant | T/C | snv | 0.49 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
3 | 0.925 | 0.040 | 8 | 16992890 | 3 prime UTR variant | G/A | snv | 5.5E-02 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
|
2 | 0.925 | 0.040 | 8 | 16992989 | 3 prime UTR variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||
|
2 | 0.925 | 0.040 | 16 | 31190398 | missense variant | C/T | snv | 1.2E-04 | 1.6E-04 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||
|
2 | 0.925 | 0.040 | 12 | 40252984 | missense variant | C/T | snv | 4.9E-04 | 2.4E-04 | 0.010 | < 0.001 | 1 | 2018 | 2018 | |||
|
4 | 0.925 | 0.080 | X | 152652814 | missense variant | A/C;T | snv | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||
|
2 | 0.925 | 0.040 | 16 | 31190282 | missense variant | G/A | snv | 7.6E-05 | 4.9E-05 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||
|
1 | 1.000 | 0.040 | 4 | 5126432 | intron variant | T/C | snv | 0.24 | 0.730 | 1.000 | 3 | 2016 | 2018 | ||||
|
1 | 1.000 | 0.040 | 10 | 67085957 | intron variant | T/G | snv | 0.35 | 0.720 | 0.667 | 3 | 2016 | 2018 | ||||
|
1 | 1.000 | 0.040 | 4 | 24360918 | intergenic variant | T/C | snv | 0.18 | 0.730 | 0.667 | 3 | 2016 | 2018 | ||||
|
1 | 1.000 | 0.040 | 10 | 67090661 | intron variant | A/G;T | snv | 0.020 | 0.500 | 2 | 2017 | 2018 | |||||
|
1 | 1.000 | 0.040 | 10 | 67157406 | intron variant | A/G | snv | 0.63 | 0.020 | 1.000 | 2 | 2017 | 2018 |