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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
34 | 0.742 | 0.400 | 16 | 5079077 | missense variant | C/G;T | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
60 | 0.689 | 0.400 | 6 | 42978878 | stop gained | C/T | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
3 | 0.925 | 0.120 | 10 | 93777592 | missense variant | C/T | snv | 1.4E-05 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
34 | 0.742 | 0.400 | 16 | 5079078 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
13 | 0.851 | 0.200 | MT | 15923 | non coding transcript exon variant | A/G | snv | 0.700 | 1.000 | 4 | 1993 | 2018 | |||||
|
14 | 0.742 | 0.240 | 5 | 162101274 | synonymous variant | C/T | snv | 0.28 | 0.31 | 0.010 | 1.000 | 1 | 2016 | 2016 | |||
|
9 | 0.882 | 0.040 | 8 | 67506804 | missense variant | G/C | snv | 1.5E-03 | 1.2E-03 | 0.700 | 0 | ||||||
|
35 | 0.742 | 0.400 | 16 | 5082676 | splice region variant | A/G | snv | 1.0E-04 | 1.3E-04 | 0.700 | 0 | ||||||
|
20 | 0.724 | 0.440 | 10 | 99844450 | missense variant | C/G;T | snv | 2.4E-05; 0.34 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
2 | 1.000 | 0.080 | 11 | 117289162 | 3 prime UTR variant | A/T | snv | 0.12 | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||
|
11 | 0.827 | 0.080 | 8 | 67483807 | stop gained | C/A;T | snv | 4.0E-06; 2.0E-03 | 2.5E-03 | 0.700 | 0 | ||||||
|
64 | 0.672 | 0.400 | 6 | 42978330 | missense variant | G/A | snv | 3.6E-05 | 2.8E-05 | 0.700 | 0 | ||||||
|
12 | 0.752 | 0.200 | 10 | 87933144 | stop gained | G/A;T | snv | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||
|
10 | 0.776 | 0.240 | 12 | 32731362 | missense variant | C/T | snv | 0.700 | 1.000 | 2 | 2016 | 2016 | |||||
|
4 | 0.882 | 0.120 | 17 | 5649930 | intergenic variant | G/C | snv | 0.44 | 0.010 | 1.000 | 1 | 2017 | 2017 |