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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 1.000 | 0.040 | 7 | 121339035 | missense variant | C/G;T | snv | 0.44 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 1.000 | 0.040 | 2 | 218879152 | upstream gene variant | G/A | snv | 0.31 | 0.010 | < 0.001 | 1 | 2013 | 2013 | ||||
|
2 | 0.925 | 0.040 | 20 | 35371345 | intron variant | T/-;TT;TTT;TTTT | delins | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 1.000 | 0.040 | 9 | 115078463 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 1.000 | 0.040 | 9 | 115080028 | intron variant | A/G | snv | 0.59 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
8 | 0.790 | 0.160 | 4 | 38774870 | missense variant | T/G | snv | 0.42 | 0.41 | 0.010 | 1.000 | 1 | 2018 | 2018 | |||
|
2 | 0.925 | 0.040 | 1 | 91714361 | intron variant | C/T | snv | 4.0E-02 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
4 | 0.851 | 0.160 | 19 | 41354682 | 3 prime UTR variant | C/T | snv | 6.2E-02 | 5.9E-02 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||
|
3 | 0.882 | 0.040 | 19 | 41327879 | intron variant | G/A | snv | 2.0E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
2 | 0.925 | 0.040 | 2 | 70490521 | intron variant | A/G | snv | 0.60 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
2 | 0.925 | 0.040 | 2 | 70493874 | intron variant | A/G | snv | 0.48 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.040 | 2 | 70487661 | intron variant | T/C | snv | 0.57 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.040 | 2 | 85309292 | missense variant | G/A | snv | 4.2E-02 | 3.8E-02 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||
|
3 | 0.882 | 0.040 | 6 | 44809954 | intron variant | A/G | snv | 0.27 | 0.700 | 1.000 | 2 | 2018 | 2019 | ||||
|
2 | 0.925 | 0.040 | 6 | 45177665 | intron variant | C/G | snv | 0.33 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
10 | 0.807 | 0.240 | 4 | 87975269 | non coding transcript exon variant | T/C | snv | 0.37 | 0.010 | < 0.001 | 1 | 2015 | 2015 | ||||
|
4 | 0.925 | 0.040 | 4 | 87975555 | non coding transcript exon variant | -/G | delins | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
1 | 1.000 | 0.040 | 7 | 129203569 | missense variant | C/T | snv | 4.1E-04 | 3.5E-04 | 0.710 | 1.000 | 1 | 2018 | 2018 | |||
|
3 | 0.882 | 0.040 | 15 | 67078107 | intron variant | G/A | snv | 0.45 | 0.040 | 0.750 | 4 | 2010 | 2018 | ||||
|
1 | 1.000 | 0.040 | 15 | 67078168 | intron variant | C/A;G | snv | 0.700 | 1.000 | 2 | 2018 | 2019 | |||||
|
3 | 0.882 | 0.160 | 15 | 67078051 | intron variant | A/G | snv | 0.25 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
1 | 1.000 | 0.040 | 15 | 67177230 | intron variant | A/G | snv | 0.54 | 0.010 | < 0.001 | 1 | 2018 | 2018 | ||||
|
1 | 1.000 | 0.040 | 4 | 1715043 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
2 | 0.925 | 0.040 | 4 | 1702517 | intron variant | T/C | snv | 0.16 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
2 | 0.925 | 0.040 | 21 | 29021343 | upstream gene variant | A/T | snv | 0.66 | 0.700 | 1.000 | 1 | 2018 | 2018 |