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 | 3 | 49855463 | intron variant | A/G | snv | 0.24 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
3 | 14 | 72996771 | intron variant | G/A | snv | 0.33 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 17 | 73199810 | intron variant | C/T | snv | 0.52 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 8 | 119736926 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1 | 7 | 21489977 | intron variant | A/C | snv | 0.33 | 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 | ||||||
|
3 | 11 | 65583893 | non coding transcript exon variant | G/A | snv | 0.20 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 2 | 10059474 | intron variant | A/G | snv | 0.59 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 2 | 54572462 | intron variant | G/T | snv | 0.31 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 12 | 26413499 | intron variant | A/C | snv | 4.7E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 7 | 47595969 | intergenic variant | T/A | snv | 0.65 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
18 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 4 | 147536174 | intron variant | T/G | snv | 0.21 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 15 | 101528701 | upstream gene variant | C/T | snv | 0.20 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 19 | 32871878 | upstream gene variant | C/T | snv | 0.36 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 10 | 88550323 | intron variant | T/A;C | snv | 0.45 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 14 | 85653458 | 3 prime UTR variant | C/T | snv | 0.27 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 7 | 50626161 | intron variant | G/A | snv | 8.8E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 1 | 213793544 | intron variant | T/C | snv | 0.45 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 4 | 156921244 | intron variant | A/G | snv | 0.50 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
4 | 0.882 | 0.080 | 1 | 15524118 | missense variant | G/A | snv | 0.50 | 0.59 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||
|
1 | 20 | 53943587 | 3 prime UTR variant | A/G | snv | 0.38 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 11 | 308290 | missense variant | T/C | snv | 0.70 | 0.70 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 3 | 194960568 | regulatory region variant | G/A | snv | 0.36 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
3 | 10 | 63559006 | intron variant | G/T | snv | 0.51 | 0.700 | 1.000 | 1 | 2019 | 2019 |