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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
8 | 0.925 | 3 | 46410189 | intron variant | A/C;G;T | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
5 | 0.925 | 11 | 119032329 | upstream gene variant | T/A;G | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
7 | 0.851 | 0.040 | 14 | 22168978 | synonymous variant | C/T | snv | 0.19 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
5 | 0.925 | 11 | 62293877 | downstream gene variant | G/A | snv | 0.29 | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
5 | 0.925 | 16 | 13267554 | intron variant | G/A | snv | 0.22 | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
6 | 0.882 | 0.080 | 9 | 19469848 | intergenic variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
5 | 0.925 | 19 | 8066356 | intron variant | G/A | snv | 0.14 | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
5 | 0.925 | 3 | 158893105 | intergenic variant | G/A | snv | 0.39 | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
6 | 0.882 | 0.080 | 6 | 131504454 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
5 | 0.925 | 3 | 115559835 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
5 | 0.925 | 11 | 17094129 | intron variant | T/C | snv | 6.2E-02 | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
5 | 0.925 | 3 | 1383484 | intron variant | T/C;G | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
5 | 0.925 | 7 | 25568789 | TF binding site variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||||
|
5 | 0.925 | 2 | 8037334 | intron variant | G/T | snv | 0.13 | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
5 | 0.925 | 7 | 126684537 | intron variant | A/G | snv | 0.13 | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||
|
9 | 0.827 | 0.080 | 15 | 33613209 | missense variant | A/G | snv | 0.23 | 0.21 | 0.700 | 1.000 | 1 | 2010 | 2010 | |||
|
6 | 0.882 | 0.120 | 6 | 31352761 | intron variant | C/T | snv | 0.53 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
5 | 0.925 | 16 | 79580219 | regulatory region variant | T/C;G | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||||
|
6 | 0.882 | 0.080 | 17 | 73383923 | missense variant | G/A | snv | 5.3E-02 | 6.3E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | |||
|
6 | 0.882 | 0.080 | 11 | 33436311 | intron variant | A/G | snv | 4.4E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
5 | 0.925 | 5 | 138446426 | 3 prime UTR variant | T/G | snv | 0.56 | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
5 | 0.925 | 6 | 31403294 | intron variant | C/A | snv | 3.3E-02 | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
5 | 0.925 | 6 | 95928822 | intron variant | A/T | snv | 0.95 | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
5 | 0.925 | 21 | 31133966 | intron variant | A/G | snv | 0.12 | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
5 | 0.925 | 2 | 109433263 | intron variant | A/G | snv | 0.51 | 0.700 | 1.000 | 1 | 2017 | 2017 |