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 | 0.882 | 0.040 | 7 | 55067179 | intron variant | A/G | snv | 0.53 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
3 | 0.882 | 0.080 | 7 | 55073624 | intron variant | T/C | snv | 0.31 | 0.010 | < 0.001 | 1 | 2017 | 2017 | ||||
|
4 | 0.882 | 0.040 | 7 | 55080369 | intron variant | AA/-;A;AAA;AAAA;AAAAAAAAAAA | delins | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
5 | 0.882 | 0.040 | 7 | 55091656 | intron variant | A/G;T | snv | 0.20 | 0.850 | 1.000 | 6 | 2011 | 2018 | ||||
|
2 | 0.925 | 0.040 | 7 | 55120299 | intron variant | G/A | snv | 0.50 | 0.010 | < 0.001 | 1 | 2017 | 2017 | ||||
|
1 | 1.000 | 0.040 | 7 | 55125270 | intron variant | T/G | snv | 0.51 | 0.010 | < 0.001 | 1 | 2017 | 2017 | ||||
|
2 | 0.925 | 0.120 | 7 | 55147325 | intron variant | A/C | snv | 0.51 | 0.040 | 0.750 | 4 | 2012 | 2017 | ||||
|
4 | 0.851 | 0.160 | 7 | 55152484 | intron variant | A/G | snv | 0.59 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 1.000 | 0.040 | 7 | 55161850 | intron variant | T/C | snv | 0.15 | 0.010 | < 0.001 | 1 | 2017 | 2017 | ||||
|
2 | 0.925 | 0.120 | 7 | 55162412 | intron variant | C/T | snv | 0.21 | 0.030 | 1.000 | 3 | 2012 | 2015 | ||||
|
1 | 1.000 | 0.040 | 7 | 55177814 | intron variant | A/G | snv | 0.43 | 0.010 | < 0.001 | 1 | 2017 | 2017 | ||||
|
48 | 0.623 | 0.280 | 7 | 55191846 | missense variant | A/T | snv | 0.010 | 1.000 | 1 | 2015 | 2015 |