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 | 2 | 224888625 | intron variant | A/G | snv | 0.24 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 17 | 74706839 | intron variant | G/A | snv | 0.53 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
3 | 19 | 53824615 | upstream gene variant | T/G | snv | 0.26 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 6 | 33080829 | missense variant | G/C | snv | 0.14 | 0.15 | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
2 | 1 | 185422035 | regulatory region variant | G/A | snv | 0.31 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 2 | 181459460 | intron variant | TT/-;T;TTT | delins | 0.56 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 11 | 306884 | upstream gene variant | T/C | snv | 0.49 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 17 | 27521170 | intron variant | C/T | snv | 0.65 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
6 | 0.882 | 19 | 18287818 | upstream gene variant | G/C | snv | 0.64 | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
2 | 10 | 97384397 | intron variant | A/G | snv | 0.30 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
3 | 1.000 | 0.040 | 10 | 99532633 | upstream gene variant | C/T | snv | 0.40 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
2 | 3 | 46323369 | intergenic variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
2 | 17 | 59850066 | upstream gene variant | TT/-;T;TTT;TTTT | delins | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
4 | 8 | 129592027 | intron variant | C/- | delins | 0.40 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
3 | 6 | 22343363 | intron variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
2 | 16 | 85902784 | 5 prime UTR variant | GGCTGCAGGT/-;GGCTGCAGGTGGCTGCAGGT;GGCTGCAGGTGGCTGCAGGTGGCTGCAGGT | delins | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
2 | 1 | 92300881 | intron variant | G/A | snv | 1.7E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
3 | 9 | 88920798 | regulatory region variant | T/C;G | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
2 | 1 | 117619797 | intron variant | C/G | snv | 0.14 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
4 | 12 | 4224753 | intergenic variant | T/C | snv | 0.22 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 16 | 85955858 | regulatory region variant | T/C;G | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
3 | 16 | 85982722 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
2 | 2 | 226426699 | intergenic variant | A/C | snv | 0.13 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 4 | 144137143 | intron variant | G/T | snv | 0.36 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 19 | 13065914 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 |