| 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 | 8 | 102236572 | intron variant | T/C | snv | 0.10 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
34 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
2 | 1 | 10248900 | intron variant | C/T | snv | 9.3E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 10 | 102506502 | intron variant | C/T | snv | 3.7E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
4 | 0.882 | 0.080 | 4 | 102537720 | non coding transcript exon variant | G/A | snv | 0.69 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 14 | 102775462 | upstream gene variant | T/C | snv | 0.47 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
5 | 0.925 | 0.120 | 10 | 102836092 | intron variant | G/A;C;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 8 | 102864097 | 5 prime UTR variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1 | 11 | 103020694 | intergenic variant | A/C | snv | 1.5E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 5 | 103264823 | intron variant | G/A | snv | 0.31 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 8 | 103390144 | intergenic variant | C/A | snv | 5.2E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 14 | 103541218 | downstream gene variant | A/G | snv | 0.71 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 11 | 10364929 | intron variant | T/C | snv | 0.73 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 14 | 103806421 | intron variant | G/A | snv | 1.3E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 10 | 103960975 | intergenic variant | G/A | snv | 0.24 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 12 | 10428441 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1 | 14 | 105134327 | intron variant | C/T | snv | 8.3E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
28 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 14 | 105288195 | intron variant | T/C | snv | 0.30 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 16 | 10531048 | 3 prime UTR variant | T/C | snv | 0.50 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
9 | 0.925 | 0.080 | 8 | 105569300 | intron variant | A/T | snv | 0.31 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
2 | 1.000 | 0.080 | 19 | 1056493 | missense variant | G/C;T | snv | 0.84; 4.1E-06 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 20 | 10638366 | 3 prime UTR variant | A/C | snv | 0.27 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 11 | 10645728 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
3 | 6 | 106725104 | non coding transcript exon variant | T/C | snv | 0.16 | 0.700 | 1.000 | 1 | 2019 | 2019 |