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 | 6 | 31272468 | intron variant | -/TC | delins | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 6 | 31356750 | missense variant | T/C;G | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 6 | 31328592 | intron variant | A/C | snv | 1.2E-02 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 6 | 31316290 | intron variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
2 | 1.000 | 0.040 | 6 | 31296356 | intron variant | G/C;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||
|
2 | 1.000 | 0.040 | 6 | 31295745 | intron variant | C/A;G | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||
|
2 | 1.000 | 0.040 | 6 | 31295733 | intron variant | T/C | snv | 0.81 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
1 | 6 | 31356979 | missense variant | G/A | snv | 3.6E-02 | 7.5E-02 | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||
|
1 | 6 | 31285529 | intron variant | AA/-;A;AAA;AAAA | delins | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 6 | 31347810 | intron variant | G/T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
9 | 0.851 | 0.200 | 6 | 31304484 | intron variant | C/T | snv | 0.81 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
2 | 1.000 | 0.080 | 6 | 31303790 | intron variant | A/G | snv | 0.80 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
1 | 6 | 31303299 | intron variant | G/C | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 6 | 31329803 | intron variant | C/T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 |