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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
11 | 0.763 | 0.200 | 8 | 129673211 | intron variant | T/G | snv | 0.17 | 0.900 | 1.000 | 12 | 2009 | 2020 | ||||
|
5 | 0.851 | 0.120 | 8 | 129479506 | intron variant | T/G | snv | 0.17 | 0.810 | 1.000 | 3 | 2009 | 2019 | ||||
|
16 | 0.732 | 0.080 | 8 | 129633446 | intron variant | A/G | snv | 3.9E-02 | 0.760 | 1.000 | 9 | 2013 | 2019 | ||||
|
3 | 0.882 | 0.040 | 8 | 129629675 | intron variant | A/G | snv | 0.18 | 0.720 | 1.000 | 4 | 2009 | 2019 | ||||
|
3 | 0.882 | 0.040 | 8 | 129465577 | intron variant | C/T | snv | 0.80 | 0.700 | 1.000 | 2 | 2009 | 2011 | ||||
|
1 | 1.000 | 0.040 | 8 | 129653397 | intron variant | G/A | snv | 0.19 | 0.700 | 1.000 | 2 | 2009 | 2011 | ||||
|
1 | 1.000 | 0.040 | 8 | 129651264 | intron variant | A/G | snv | 0.34 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||
|
1 | 1.000 | 0.040 | 8 | 129627294 | non coding transcript exon variant | G/A | snv | 0.30 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||
|
1 | 1.000 | 0.040 | 8 | 129666930 | intron variant | A/G | snv | 0.34 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||
|
1 | 1.000 | 0.040 | 8 | 129652161 | intron variant | T/C | snv | 0.37 | 0.700 | 1.000 | 1 | 2011 | 2011 |