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 | 0.040 | 7 | 25123996 | missense variant | C/T | snv | 0.710 | 1.000 | 1 | 2014 | 2019 | |||||
|
4 | 0.851 | 0.120 | 12 | 11869601 | missense variant | C/T | snv | 0.710 | 1.000 | 1 | 2015 | 2015 | |||||
|
4 | 0.882 | 0.120 | 12 | 11884481 | missense variant | T/C | snv | 0.710 | 1.000 | 1 | 2015 | 2015 | |||||
|
1 | 0.925 | 0.040 | 20 | 37403347 | missense variant | G/A | snv | 0.710 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 10 | 118867050 | intron variant | A/G | snv | 0.52 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
|
2 | 1.000 | 0.040 | 9 | 113262744 | 3 prime UTR variant | A/C | snv | 0.47 | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||
|
1 | 10 | 103138228 | intron variant | T/C;G | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1 | 9 | 134060541 | intron variant | G/T | snv | 0.14 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 0.851 | 0.080 | 17 | 4933119 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||
|
21 | 0.716 | 0.400 | 1 | 155236354 | missense variant | T/C | snv | 1.4E-05 | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||
|
1 | 3 | 129062206 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
4 | 0.882 | 0.120 | X | 154365245 | missense variant | C/A;G;T | snv | 3.1E-03 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
3 | 0.925 | 0.040 | 11 | 59457412 | missense variant | G/A;C | snv | 7.2E-05; 0.26 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
|
3 | 0.925 | 0.040 | 3 | 119782192 | 5 prime UTR variant | C/A | snv | 0.48 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
1 | 3 | 119780660 | 5 prime UTR variant | T/C | snv | 0.47 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
|
4 | 0.882 | 0.120 | 1 | 11788011 | missense variant | G/C | snv | 0.10 | 0.10 | 0.010 | 1.000 | 1 | 2014 | 2014 | |||
|
2 | 1.000 | 0.040 | 8 | 89644760 | intron variant | T/C | snv | 0.55 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 12 | 112663189 | intron variant | C/A | snv | 0.26 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
|
2 | 1.000 | 0.080 | 4 | 54228462 | intron variant | G/C;T | snv | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||
|
29 | 0.658 | 0.400 | 1 | 206776020 | intron variant | A/T | snv | 0.32 | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||
|
92 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 0.010 | 1.000 | 1 | 2014 | 2014 | |||
|
169 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 0.010 | 1.000 | 1 | 2014 | 2014 | |||
|
12 | 0.763 | 0.280 | 1 | 97883329 | missense variant | A/G | snv | 0.28 | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.925 | 0.160 | 8 | 127736777 | intron variant | G/T | snv | 7.1E-02 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
2 | 1.000 | 0.040 | 8 | 89688709 | intron variant | C/T | snv | 0.67 | 0.010 | 1.000 | 1 | 2019 | 2019 |