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 | 14 | 61717464 | intron variant | A/G | snv | 8.8E-02 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 15 | 86311359 | intron variant | A/C | snv | 0.28 | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||
|
1 | 2 | 238975165 | regulatory region variant | A/G | snv | 0.39 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 7 | 158000430 | intron variant | G/A;C;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1 | 4 | 147539622 | intron variant | T/C | snv | 2.1E-02 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 19 | 19609015 | intron variant | C/G | snv | 0.45 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 19 | 6836678 | intron variant | C/T | snv | 2.5E-02 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 15 | 43724219 | downstream gene variant | T/C | snv | 0.16 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 14 | 64245143 | intron variant | A/G | snv | 4.4E-03 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 11 | 116739533 | regulatory region variant | A/G | snv | 0.17 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 5 | 75321018 | intron variant | T/C | snv | 0.36 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||
|
1 | 5 | 173227744 | upstream gene variant | T/C | snv | 2.1E-02 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 2 | 20973240 | intergenic variant | A/G | snv | 0.77 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||
|
1 | 5 | 75600973 | 3 prime UTR variant | G/A | snv | 0.22 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||
|
1 | 15 | 58520578 | intron variant | C/T | snv | 5.4E-02 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 4 | 148230877 | intron variant | C/G | snv | 1.6E-02 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 22 | 32862301 | 3 prime UTR variant | T/C | snv | 0.29 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 12 | 109532300 | intron variant | G/A | snv | 9.1E-03 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 11 | 122327998 | intron variant | A/G | snv | 0.63 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1 | 11 | 78387968 | intron variant | T/G | snv | 0.15 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 11 | 113425897 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 11 | 48264704 | missense variant | C/T | snv | 0.52 | 0.46 | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
1 | 19 | 4965053 | upstream gene variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 1 | 76996050 | intron variant | A/G | snv | 0.25 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 1 | 162265600 | intron variant | C/T | snv | 0.97 | 0.700 | 1.000 | 1 | 2012 | 2012 |