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 | 1.000 | 0.080 | 8 | 93011994 | intron variant | T/G | snv | 0.24 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
1 | 8 | 144842937 | stop gained | C/G;T | snv | 1.6E-05; 0.31 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
2 | 1.000 | 0.080 | 9 | 88973603 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||
|
1 | 9 | 86078634 | intron variant | G/A | snv | 1.9E-02 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
2 | 1.000 | 0.080 | 9 | 90331096 | intron variant | G/A | snv | 0.44 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
1 | 10 | 52058389 | intron variant | A/C;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
2 | 1.000 | 0.080 | 11 | 79730650 | intergenic variant | T/C | snv | 0.18 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
1 | 11 | 5270506 | intron variant | C/T | snv | 0.11 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 11 | 1749985 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 12 | 69662005 | intron variant | C/T | snv | 1.2E-02 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 12 | 60075450 | intergenic variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 12 | 97789941 | intergenic variant | G/A | snv | 0.20 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 12 | 104410836 | regulatory region variant | G/C | snv | 5.0E-02 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 13 | 48839332 | regulatory region variant | C/T | snv | 0.31 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 13 | 32663326 | intron variant | C/A;G | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 13 | 61728432 | regulatory region variant | A/G | snv | 0.23 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
1 | 14 | 53804550 | intron variant | A/G | snv | 1.0E-02 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 14 | 97119552 | intron variant | G/A | snv | 0.12 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 14 | 39556042 | intron variant | C/T | snv | 0.77 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 15 | 39602982 | intron variant | A/T | snv | 8.3E-03 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 15 | 87284961 | intergenic variant | A/C | snv | 2.9E-02 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 15 | 67858585 | intron variant | A/G;T | snv | 0.77 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
1 | 15 | 65741731 | synonymous variant | A/C | snv | 2.6E-02 | 2.4E-02 | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||
|
1 | 16 | 26440122 | intergenic variant | T/C | snv | 0.16 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
1 | 16 | 69282015 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 |