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 | 0.776 | 0.200 | 9 | 27543283 | non coding transcript exon variant | T/A;C | snv | 0.870 | 1.000 | 5 | 2009 | 2018 | |||||
|
2 | 0.882 | 0.120 | 9 | 27536399 | non coding transcript exon variant | C/G;T | snv | 0.830 | 1.000 | 3 | 2009 | 2014 | |||||
|
1 | 1.000 | 0.080 | 9 | 27556782 | synonymous variant | G/A | snv | 0.24 | 0.21 | 0.800 | 1.000 | 1 | 2010 | 2010 | |||
|
1 | 1.000 | 0.080 | 9 | 27561051 | 3 prime UTR variant | T/C | snv | 0.23 | 0.700 | 1.000 | 2 | 2010 | 2013 | ||||
|
1 | 1.000 | 0.080 | 9 | 27557921 | intron variant | T/C | snv | 0.20 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 1.000 | 0.080 | 9 | 27542263 | non coding transcript exon variant | C/T | snv | 0.42 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 1.000 | 0.080 | 9 | 27544945 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
1 | 1.000 | 0.080 | 9 | 27553878 | intron variant | T/C | snv | 0.20 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 1.000 | 0.080 | 9 | 27559735 | non coding transcript exon variant | G/A | snv | 0.43 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 1.000 | 0.080 | 9 | 27572636 | intron variant | C/T | snv | 0.23 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 1.000 | 0.080 | 9 | 27572257 | intron variant | C/A | snv | 0.38 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 1.000 | 0.080 | 9 | 27572636 | intron variant | -/GGAAAGTGCAGGACCTCCCTCCTG | delins | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
1 | 1.000 | 0.080 | 9 | 27559837 | non coding transcript exon variant | G/A | snv | 0.21 | 0.700 | 1.000 | 1 | 2013 | 2013 |