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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
10 | 0.882 | 0.200 | 17 | 61379228 | non coding transcript exon variant | C/T | snv | 0.69 | 0.700 | 1.000 | 5 | 2010 | 2018 | ||||
|
4 | 1.000 | 0.080 | 6 | 160247357 | intron variant | A/G;T | snv | 0.700 | 1.000 | 4 | 2010 | 2019 | |||||
|
4 | 1.000 | 0.080 | 15 | 45349027 | intergenic variant | C/A | snv | 0.56 | 0.700 | 1.000 | 3 | 2010 | 2017 | ||||
|
5 | 0.925 | 0.120 | 5 | 177386403 | intron variant | C/T | snv | 0.23 | 0.20 | 0.700 | 1.000 | 3 | 2017 | 2018 | |||
|
7 | 1.000 | 0.080 | 11 | 30738788 | intergenic variant | T/C | snv | 0.35 | 0.700 | 1.000 | 3 | 2016 | 2019 | ||||
|
7 | 1.000 | 0.080 | 16 | 20381010 | intron variant | G/A | snv | 0.16 | 0.700 | 1.000 | 3 | 2017 | 2019 | ||||
|
7 | 0.882 | 0.200 | 6 | 43838872 | intron variant | G/A;C | snv | 0.700 | 1.000 | 3 | 2010 | 2018 | |||||
|
5 | 1.000 | 0.080 | 8 | 23893638 | regulatory region variant | C/T | snv | 0.37 | 0.700 | 1.000 | 2 | 2010 | 2016 | ||||
|
34 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 0.700 | 1.000 | 2 | 2017 | 2019 | |||
|
4 | 1.000 | 0.080 | 12 | 240132 | intron variant | C/T | snv | 0.57 | 0.700 | 1.000 | 2 | 2010 | 2016 | ||||
|
4 | 1.000 | 0.080 | 10 | 1110225 | intron variant | T/C | snv | 0.89 | 0.700 | 1.000 | 2 | 2010 | 2016 | ||||
|
4 | 1.000 | 0.080 | 5 | 39397030 | intron variant | T/A | snv | 0.39 | 0.700 | 1.000 | 2 | 2010 | 2016 | ||||
|
4 | 1.000 | 0.080 | 19 | 32865985 | intron variant | T/C | snv | 0.36 | 0.700 | 1.000 | 2 | 2010 | 2016 | ||||
|
81 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 0.700 | 1.000 | 2 | 2010 | 2016 | |||
|
11 | 0.827 | 0.200 | 16 | 20356368 | upstream gene variant | G/T | snv | 0.14 | 0.700 | 1.000 | 2 | 2010 | 2016 | ||||
|
6 | 1.000 | 0.040 | 4 | 76490987 | intron variant | G/A | snv | 0.33 | 0.700 | 1.000 | 2 | 2017 | 2019 | ||||
|
5 | 1.000 | 0.080 | 2 | 73641201 | missense variant | A/G | snv | 0.21 | 0.31 | 0.700 | 1.000 | 2 | 2010 | 2016 | |||
|
7 | 0.882 | 0.200 | 15 | 75866642 | intron variant | G/A;T | snv | 0.700 | 1.000 | 2 | 2010 | 2016 | |||||
|
5 | 0.925 | 0.080 | 4 | 76447694 | intron variant | G/A | snv | 0.34 | 0.700 | 1.000 | 2 | 2010 | 2016 | ||||
|
4 | 1.000 | 0.080 | 15 | 45406595 | intron variant | T/A;G | snv | 0.700 | 1.000 | 2 | 2016 | 2019 | |||||
|
7 | 0.925 | 0.120 | 1 | 150979001 | upstream gene variant | T/C | snv | 0.14 | 0.700 | 1.000 | 2 | 2010 | 2016 | ||||
|
4 | 1.000 | 0.080 | 3 | 142088295 | intron variant | C/A | snv | 0.74 | 0.700 | 1.000 | 2 | 2010 | 2016 | ||||
|
3 | 1 | 201047168 | missense variant | G/A | snv | 0.12 | 8.9E-02 | 0.700 | 1.000 | 2 | 2016 | 2017 | |||||
|
7 | 0.882 | 0.200 | 11 | 65739351 | intergenic variant | C/G | snv | 0.31 | 0.700 | 1.000 | 2 | 2010 | 2016 | ||||
|
4 | 1.000 | 0.080 | 9 | 68819791 | intron variant | A/C;T | snv | 0.700 | 1.000 | 2 | 2010 | 2016 |