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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 1.000 | 0.040 | 9 | 32523739 | intron variant | T/C | snv | 0.41 | 0.800 | 1.000 | 3 | 2012 | 2015 | ||||
|
1 | 1.000 | 0.040 | 12 | 56045425 | upstream gene variant | A/G | snv | 0.14 | 0.800 | 1.000 | 3 | 2010 | 2015 | ||||
|
1 | 1.000 | 0.040 | 6 | 111352511 | intron variant | T/A;C | snv | 0.800 | 1.000 | 3 | 2010 | 2015 | |||||
|
1 | 1.000 | 0.040 | 1 | 24191716 | upstream gene variant | T/C | snv | 0.68 | 0.700 | 1.000 | 2 | 2015 | 2015 | ||||
|
1 | 1.000 | 0.040 | 14 | 35212966 | intron variant | T/C | snv | 0.19 | 0.800 | 1.000 | 2 | 2010 | 2015 | ||||
|
1 | 1.000 | 0.040 | 6 | 31142614 | missense variant | G/A;C | snv | 4.0E-06; 0.28 | 0.710 | 1.000 | 2 | 2011 | 2019 | ||||
|
1 | 1.000 | 0.040 | 7 | 37346633 | intron variant | C/A | snv | 0.60 | 0.800 | 1.000 | 2 | 2012 | 2015 | ||||
|
1 | 1.000 | 0.040 | 13 | 20188817 | 3 prime UTR variant | A/G | snv | 0.74 | 0.710 | 1.000 | 2 | 2010 | 2012 | ||||
|
1 | 1.000 | 0.040 | 6 | 111334327 | intron variant | G/A | snv | 8.7E-02 | 0.800 | 1.000 | 2 | 2010 | 2015 | ||||
|
1 | 1.000 | 0.040 | 6 | 137874556 | intron variant | T/C | snv | 0.70 | 0.700 | 1.000 | 2 | 2015 | 2015 | ||||
|
1 | 1.000 | 0.040 | 19 | 52948038 | intron variant | T/C | snv | 0.42 | 0.800 | 1.000 | 2 | 2010 | 2015 | ||||
|
1 | 1.000 | 0.040 | 8 | 103931366 | missense variant | T/C | snv | 0.010 | 1.000 | 1 | 2008 | 2008 | |||||
|
1 | 1.000 | 0.040 | 8 | 3826677 | intron variant | C/T | snv | 0.76 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
1 | 1.000 | 0.040 | 20 | 45352086 | upstream gene variant | T/C | snv | 0.79 | 0.800 | 1.000 | 1 | 2010 | 2010 | ||||
|
1 | 1.000 | 0.040 | 2 | 85699222 | downstream gene variant | C/T | snv | 0.31 | 0.010 | < 0.001 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.040 | 19 | 1312729 | intergenic variant | G/A | snv | 7.9E-02 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
1 | 1.000 | 0.040 | 1 | 67238424 | intron variant | G/A | snv | 0.43 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 1.000 | 0.040 | 5 | 159231004 | intron variant | A/G | snv | 0.13 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
1 | 1.000 | 0.040 | 19 | 10467167 | missense variant | C/A;T | snv | 0.17; 4.8E-05 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
1 | 1.000 | 0.040 | 1 | 67239891 | intron variant | C/T | snv | 0.62 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 1.000 | 0.040 | 1 | 152565478 | downstream gene variant | G/A | snv | 0.48 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
1 | 1.000 | 0.040 | 9 | 12483941 | intergenic variant | A/C | snv | 9.4E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.040 | 9 | 108054739 | regulatory region variant | A/G | snv | 0.44 | 0.800 | 1.000 | 1 | 2012 | 2012 | ||||
|
1 | 1.000 | 0.040 | 12 | 10444608 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
1 | 1.000 | 0.040 | 12 | 122183779 | intron variant | G/A | snv | 0.43 | 0.700 | 1.000 | 1 | 2017 | 2017 |