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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
9 | 0.882 | 0.120 | 11 | 27645655 | intron variant | T/G | snv | 0.72 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
15 | 0.752 | 0.160 | 11 | 27678578 | intron variant | C/T | snv | 0.82 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
272 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 0.700 | 1.000 | 7 | 2009 | 2019 | |||
|
3 | 11 | 27635242 | intron variant | G/T | snv | 0.20 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
3 | 1.000 | 0.080 | 11 | 27672694 | intron variant | G/A;C | snv | 0.13 | 0.700 | 1.000 | 2 | 2017 | 2019 | ||||
|
3 | 11 | 27680836 | intron variant | G/T | snv | 0.16 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
12 | 0.790 | 0.240 | 11 | 27662970 | intron variant | A/G | snv | 0.16 | 0.700 | 1.000 | 6 | 2014 | 2019 | ||||
|
2 | 11 | 27660049 | non coding transcript exon variant | C/G | snv | 0.19 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
2 | 1.000 | 0.080 | 11 | 27656039 | 3 prime UTR variant | G/T | snv | 0.17 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
2 | 11 | 27618676 | intron variant | T/G | snv | 0.73 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 11 | 27648561 | intron variant | T/C | snv | 0.17 | 0.700 | 1.000 | 1 | 2017 | 2017 |