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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
5 | 0.925 | 0.120 | 15 | 76012162 | 5 prime UTR variant | A/G | snv | 0.18 | 0.700 | 1.000 | 4 | 2017 | 2019 | ||||
|
3 | 12 | 75877403 | intron variant | G/A | snv | 0.40 | 0.700 | 1.000 | 4 | 2018 | 2019 | ||||||
|
3 | 1.000 | 0.080 | 18 | 26813249 | intron variant | C/A;T | snv | 0.700 | 1.000 | 4 | 2018 | 2019 | |||||
|
2 | 1.000 | 0.080 | 9 | 68817258 | intron variant | G/A | snv | 0.63 | 0.700 | 1.000 | 4 | 2019 | 2019 | ||||
|
4 | 1.000 | 0.040 | 1 | 150968149 | missense variant | T/A;G | snv | 4.0E-06; 0.15 | 0.700 | 1.000 | 4 | 2017 | 2019 | ||||
|
5 | 0.925 | 0.120 | 5 | 177386403 | intron variant | C/T | snv | 0.23 | 0.20 | 0.700 | 1.000 | 4 | 2017 | 2019 | |||
|
2 | 7 | 155871992 | intergenic variant | C/A;T | snv | 0.40 | 0.700 | 1.000 | 4 | 2017 | 2019 | ||||||
|
3 | 7 | 151717243 | intron variant | T/A;C | snv | 0.700 | 1.000 | 3 | 2016 | 2019 | |||||||
|
5 | 0.925 | 0.120 | 10 | 50885488 | intron variant | G/A | snv | 0.19 | 0.700 | 1.000 | 3 | 2017 | 2019 | ||||
|
2 | 5 | 68443447 | regulatory region variant | G/A;T | snv | 8.7E-02 | 0.700 | 1.000 | 3 | 2017 | 2019 | ||||||
|
1 | 1 | 112716059 | non coding transcript exon variant | T/C | snv | 8.9E-02 | 0.700 | 1.000 | 3 | 2019 | 2019 | ||||||
|
2 | 16 | 51721080 | intergenic variant | T/C | snv | 0.23 | 0.700 | 1.000 | 3 | 2018 | 2019 | ||||||
|
6 | 1.000 | 0.040 | 4 | 76490987 | intron variant | G/A | snv | 0.33 | 0.700 | 1.000 | 3 | 2017 | 2019 | ||||
|
9 | 0.882 | 0.120 | 2 | 120548864 | upstream gene variant | G/A | snv | 0.33 | 0.700 | 1.000 | 3 | 2016 | 2019 | ||||
|
1 | 18 | 5585159 | intron variant | A/G | snv | 0.37 | 0.700 | 1.000 | 3 | 2019 | 2019 | ||||||
|
4 | 1.000 | 0.080 | 2 | 176128855 | intron variant | C/G | snv | 1.5E-02 | 1.5E-02 | 0.700 | 1.000 | 3 | 2017 | 2019 | |||
|
2 | 1.000 | 0.040 | 20 | 34941963 | intron variant | T/G | snv | 0.52 | 0.700 | 1.000 | 3 | 2019 | 2019 | ||||
|
4 | 18 | 48934533 | intron variant | C/A;G | snv | 0.700 | 1.000 | 3 | 2018 | 2019 | |||||||
|
5 | 1.000 | 0.080 | 21 | 15204463 | intron variant | G/A | snv | 0.34 | 0.700 | 1.000 | 3 | 2019 | 2019 | ||||
|
2 | 21 | 33984405 | regulatory region variant | G/A | snv | 0.11 | 0.700 | 1.000 | 3 | 2019 | 2019 | ||||||
|
7 | 1.000 | 0.080 | 11 | 30738788 | intergenic variant | T/C | snv | 0.35 | 0.700 | 1.000 | 3 | 2016 | 2019 | ||||
|
4 | 1.000 | 0.080 | 9 | 68819791 | intron variant | A/C;T | snv | 0.700 | 1.000 | 3 | 2016 | 2019 | |||||
|
5 | 20 | 54114863 | intergenic variant | A/T | snv | 0.28 | 0.700 | 1.000 | 3 | 2017 | 2019 | ||||||
|
1 | 12 | 3283185 | 3 prime UTR variant | A/G | snv | 0.44 | 0.700 | 1.000 | 3 | 2019 | 2019 | ||||||
|
1 | 8 | 23862058 | TF binding site variant | C/A;G;T | snv | 0.700 | 1.000 | 3 | 2019 | 2019 |