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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
13 | 1.000 | 0.080 | 11 | 61837342 | intron variant | C/A | snv | 0.38 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
8 | 1.000 | 0.040 | 17 | 46935905 | 3 prime UTR variant | T/C | snv | 9.2E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
2 | 13 | 73946049 | intron variant | T/A | snv | 0.40 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 2 | 174603041 | intron variant | T/C | snv | 0.79 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
3 | 20 | 34952197 | 5 prime UTR variant | G/A | snv | 0.19 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 3 | 38518258 | intron variant | A/C;G | snv | 0.23 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 1 | 61432295 | intron variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
2 | 3 | 66381178 | intron variant | A/C;G | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
2 | 1.000 | 0.040 | 17 | 45949373 | intron variant | G/A | snv | 0.35 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
1 | 1 | 26060932 | intron variant | G/A | snv | 0.24 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 5 | 173888863 | 5 prime UTR variant | C/G | snv | 0.11 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 2 | 36965723 | intron variant | C/T | snv | 0.18 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 6 | 12159466 | intron variant | C/T | snv | 0.23 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 20 | 6479643 | intron variant | C/T | snv | 0.84 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 1 | 115768346 | missense variant | T/C | snv | 0.33 | 0.34 | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
3 | 1.000 | 0.080 | 3 | 12800724 | intron variant | T/G | snv | 0.63 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
2 | 3 | 53248287 | intron variant | A/G | snv | 0.75 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 6 | 159472905 | intron variant | G/T | snv | 0.31 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 1 | 3342619 | intron variant | A/G | snv | 6.8E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
7 | 1.000 | 0.080 | 3 | 38725824 | intron variant | T/C | snv | 0.67 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
1 | 7 | 46601302 | intergenic variant | C/T | snv | 0.61 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 12 | 114943266 | intergenic variant | T/C | snv | 0.27 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 16 | 11595035 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1 | 17 | 30158744 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1 | 21 | 15754675 | intron variant | G/A | snv | 0.23 | 0.700 | 1.000 | 1 | 2016 | 2016 |