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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 1.000 | 0.040 | 4 | 61608511 | intron variant | C/A | snv | 0.55 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
27 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||
|
28 | 0.672 | 0.400 | 13 | 20189511 | stop gained | C/T | snv | 5.8E-04 | 1.1E-04 | 0.700 | 0 | ||||||
|
2 | 0.925 | 0.040 | 1 | 165411386 | intron variant | G/A | snv | 0.55 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
2 | 0.925 | 0.040 | 13 | 108163877 | intergenic variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2008 | 2008 | |||||
|
1 | 1.000 | 0.040 | 5 | 36686784 | 3 prime UTR variant | A/C | snv | 0.35 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
5 | 0.851 | 0.040 | 8 | 4323322 | intron variant | C/A | snv | 0.18 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||
|
41 | 0.627 | 0.640 | 21 | 45537880 | missense variant | T/C;G | snv | 0.55; 4.4E-06 | 0.030 | 1.000 | 3 | 2014 | 2018 | ||||
|
5 | 0.827 | 0.120 | 20 | 10306440 | 3 prime UTR variant | T/C | snv | 0.20 | 0.030 | 0.667 | 3 | 2007 | 2013 | ||||
|
1 | 1.000 | 0.040 | 16 | 84412778 | intron variant | C/A;G | snv | 0.800 | 1.000 | 1 | 2008 | 2008 | |||||
|
2 | 0.925 | 0.120 | 18 | 60371539 | missense variant | A/G | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||
|
21 | 0.851 | 0.120 | 14 | 101986552 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.080 | 9 | 87969919 | stop gained | C/G;T | snv | 4.9E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.040 | 10 | 52014152 | intron variant | T/A;C;G | snv | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||
|
1 | 1.000 | 0.040 | 10 | 52017283 | intron variant | T/G | snv | 0.51 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
1 | 1.000 | 0.040 | 10 | 52019720 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||
|
1 | 1.000 | 0.040 | 10 | 28966665 | intergenic variant | C/A | snv | 0.13 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
21 | 0.752 | 0.320 | 6 | 79025582 | missense variant | G/T | snv | 0.700 | 0 | ||||||||
|
8 | 0.807 | 0.160 | 10 | 87933128 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
7 | 0.827 | 0.160 | 10 | 87933178 | frameshift variant | -/A | delins | 0.700 | 0 | ||||||||
|
8 | 0.851 | 0.160 | 10 | 87957850 | splice region variant | C/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 11 | 115266527 | intron variant | T/G | snv | 0.33 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.040 | 1 | 232802953 | upstream gene variant | G/A | snv | 7.5E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
2 | 1.000 | 0.040 | 8 | 92392214 | intergenic variant | A/C | snv | 0.28 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.040 | 9 | 116571404 | intron variant | C/A;G | snv | 0.16 | 0.800 | 1.000 | 1 | 2008 | 2008 |