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 | 20 | 32849813 | 3 prime UTR variant | G/C | snv | 9.3E-03 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 22 | 33416876 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
4 | 6 | 27033276 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1 | 2 | 107482651 | intron variant | G/C | snv | 3.5E-03 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
4 | 6 | 25715429 | regulatory region variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
2 | 6 | 26255511 | upstream gene variant | G/A | snv | 0.10 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 7 | 23289983 | regulatory region variant | G/A | snv | 1.1E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
2 | 6 | 25373818 | intron variant | C/T | snv | 0.11 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
15 | 0.790 | 0.200 | X | 154536002 | missense variant | C/T | snv | 9.1E-03 | 3.6E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | |||
|
1 | 8 | 37125160 | intergenic variant | G/A | snv | 1.2E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 8 | 36920273 | intron variant | C/A | snv | 1.0E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 |