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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
10 | 0.827 | 0.360 | X | 124365758 | splice region variant | C/G | snv | 0.700 | 0 | ||||||||
|
4 | 0.851 | 0.080 | 1 | 92833637 | frameshift variant | AACA/- | delins | 0.700 | 0 | ||||||||
|
4 | 0.882 | 0.160 | 22 | 17209534 | frameshift variant | C/-;CC | delins | 0.700 | 0 | ||||||||
|
25 | 0.776 | 0.360 | 9 | 127825225 | splice region variant | A/G | snv | 8.0E-06 | 0.700 | 0 | |||||||
|
4 | 0.851 | 0.120 | 8 | 6465757 | intron variant | G/A | snv | 0.28 | 0.810 | 1.000 | 1 | 2011 | 2011 | ||||
|
3 | 0.925 | 0.160 | 16 | 53826140 | missense variant | G/A | snv | 2.1E-03 | 6.4E-04 | 0.710 | 1.000 | 1 | 2017 | 2017 | |||
|
2 | 1.000 | 0.040 | 2 | 195143585 | intergenic variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||
|
2 | 1.000 | 0.040 | 3 | 62886233 | intergenic variant | C/A;G;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||
|
2 | 1.000 | 0.040 | 1 | 212668592 | upstream gene variant | T/C | snv | 0.24 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
4 | 0.851 | 0.200 | 2 | 136114928 | stop gained | G/A | snv | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||
|
3 | 0.925 | 0.040 | 21 | 45530803 | missense variant | C/T | snv | 1.1E-05 | 7.0E-06 | 0.010 | 1.000 | 1 | 2016 | 2016 | |||
|
8 | 0.807 | 0.160 | 10 | 95038992 | missense variant | T/C | snv | 8.3E-02 | 8.0E-02 | 0.010 | 1.000 | 1 | 2014 | 2014 | |||
|
41 | 0.627 | 0.640 | 21 | 45537880 | missense variant | T/C;G | snv | 0.55; 4.4E-06 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
2 | 0.925 | 0.040 | 10 | 74176853 | 5 prime UTR variant | C/G;T | snv | 0.67 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
2 | 0.925 | 0.080 | 20 | 4874036 | synonymous variant | A/G | snv | 0.34 | 0.43 | 0.010 | 1.000 | 1 | 2014 | 2014 | |||
|
3 | 0.882 | 0.160 | 9 | 87620879 | intron variant | A/C | snv | 0.25 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
214 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||
|
490 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||
|
8 | 0.807 | 0.200 | 22 | 42126611 | missense variant | C/G | snv | 0.58 | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||
|
9 | 0.776 | 0.280 | 6 | 18130687 | missense variant | T/C;G | snv | 3.7E-02 | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||
|
27 | 0.658 | 0.560 | 9 | 117715853 | 3 prime UTR variant | G/C | snv | 0.11 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
62 | 0.572 | 0.640 | 19 | 45420395 | synonymous variant | A/G | snv | 0.50 | 0.55 | 0.010 | 1.000 | 1 | 2020 | 2020 | |||
|
3 | 0.882 | 0.080 | 3 | 49026677 | intron variant | A/G | snv | 8.3E-02 | 7.6E-02 | 0.010 | 1.000 | 1 | 2010 | 2010 | |||
|
2 | 0.925 | 0.040 | 3 | 194865359 | intergenic variant | T/C | snv | 0.53 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
2 | 0.925 | 0.040 | 1 | 65772696 | regulatory region variant | G/A | snv | 0.17 | 0.010 | 1.000 | 1 | 2012 | 2012 |