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 | 0.925 | 0.080 | 15 | 78573551 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||
|
4 | 0.882 | 0.120 | 15 | 78578946 | intron variant | T/C | snv | 0.60 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
37 | 0.653 | 0.360 | 15 | 78590583 | missense variant | G/A | snv | 0.26 | 0.24 | 0.100 | 0.963 | 27 | 2008 | 2018 | |||
|
3 | 0.882 | 0.080 | 15 | 78584808 | intron variant | A/G | snv | 0.68 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
3 | 0.882 | 0.080 | 15 | 78589276 | non coding transcript exon variant | T/C | snv | 0.28 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
9 | 0.827 | 0.120 | 15 | 78575140 | intron variant | A/C | snv | 0.32 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
3 | 0.882 | 0.080 | 15 | 78563924 | upstream gene variant | C/T | snv | 0.27 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
3 | 0.882 | 0.080 | 15 | 78585221 | intron variant | A/G | snv | 0.64 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
6 | 0.851 | 0.080 | 15 | 78565554 | 5 prime UTR variant | T/A | snv | 0.28 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
6 | 0.827 | 0.200 | 15 | 78573083 | intron variant | T/A;C | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
13 | 0.790 | 0.120 | 15 | 78571130 | intron variant | T/C | snv | 0.28 | 0.010 | < 0.001 | 1 | 2013 | 2013 |