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 | 0.790 | 0.160 | 12 | 57140687 | intron variant | G/A;C | snv | 0.840 | 1.000 | 4 | 2011 | 2015 | |||||
|
15 | 0.790 | 0.120 | 19 | 11091630 | intron variant | G/T | snv | 0.12 | 0.810 | 1.000 | 2 | 2013 | 2017 | ||||
|
4 | 0.851 | 0.040 | 9 | 121660124 | intron variant | G/A | snv | 0.28 | 0.810 | 1.000 | 1 | 2010 | 2010 | ||||
|
22 | 0.695 | 0.280 | 9 | 22115960 | intron variant | A/G | snv | 0.64 | 0.800 | 1.000 | 1 | 2010 | 2010 | ||||
|
1 | 1.000 | 0.040 | 21 | 38447907 | intron variant | C/A;T | snv | 0.720 | 1.000 | 3 | 2017 | 2020 | |||||
|
1 | 1.000 | 0.040 | 1 | 214235937 | intergenic variant | T/C;G | snv | 0.710 | 0.500 | 2 | 2017 | 2020 | |||||
|
2 | 0.925 | 0.120 | 8 | 117013406 | intron variant | T/A;G | snv | 0.710 | 1.000 | 2 | 2011 | 2015 | |||||
|
1 | 1.000 | 0.040 | 13 | 22287782 | intergenic variant | A/G | snv | 0.22 | 0.710 | 0.500 | 2 | 2017 | 2020 | ||||
|
22 | 0.701 | 0.320 | 9 | 22096056 | intron variant | A/G | snv | 0.41 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 1.000 | 0.040 | 9 | 121662964 | intron variant | C/T | snv | 0.17 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
3 | 0.925 | 0.040 | 1 | 154455807 | intron variant | A/G | snv | 0.44 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 1.000 | 0.040 | 2 | 20682689 | upstream gene variant | A/G;T | snv | 0.59 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 1.000 | 0.040 | 12 | 57138966 | intron variant | G/C | snv | 0.26 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 1.000 | 0.040 | 20 | 45942678 | intron variant | G/A;T | snv | 0.13 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
3 | 0.882 | 0.080 | 15 | 48548638 | intron variant | C/T | snv | 7.7E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
10 | 0.851 | 0.080 | 1 | 109278889 | downstream gene variant | T/G | snv | 0.63 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
3 | 0.882 | 0.080 | 9 | 22091925 | intron variant | G/T | snv | 0.50 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
3 | 0.882 | 0.080 | 18 | 22605468 | regulatory region variant | G/A | snv | 0.43 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
3 | 0.882 | 0.080 | 2 | 197301841 | intron variant | G/A | snv | 0.38 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
614 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 0.060 | 0.500 | 6 | 2003 | 2017 | |||
|
44 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 0.040 | 0.750 | 4 | 2008 | 2014 | ||||
|
174 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 0.030 | 1.000 | 3 | 2014 | 2015 | |||
|
5 | 0.827 | 0.120 | 17 | 1754359 | missense variant | G/A | snv | 0.22 | 0.20 | 0.020 | 1.000 | 2 | 2014 | 2019 | |||
|
60 | 0.614 | 0.520 | 9 | 22125504 | intron variant | G/C | snv | 0.41 | 0.020 | 1.000 | 2 | 2010 | 2014 | ||||
|
246 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 0.020 | 1.000 | 2 | 2005 | 2010 |