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 | 1 | 153928504 | intron variant | A/G;T | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
|
1 | 1.000 | 19 | 2739698 | intron variant | A/G | snv | 0.45 | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||
|
1 | 1.000 | 1 | 153966654 | non coding transcript exon variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
|
1 | 1.000 | 5 | 69113267 | non coding transcript exon variant | A/C;T | snv | 0.67; 6.1E-04 | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||
|
1 | 1.000 | 15 | 63068648 | intron variant | T/C | snv | 0.59 | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 1.000 | 9 | 95476076 | synonymous variant | G/A | snv | 0.17 | 0.15 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
1 | 1.000 | 15 | 45487612 | synonymous variant | G/A | snv | 0.71 | 0.75 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
1 | 1.000 | 1 | 228037123 | intron variant | A/G | snv | 0.61 | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||
|
1 | 1.000 | 17 | 46770948 | intron variant | G/T | snv | 0.25 | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||
|
1 | 1.000 | 13 | 68578880 | intergenic variant | T/A;G | snv | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 1.000 | 19 | 2738354 | intron variant | A/C;G;T | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
|
1 | 1.000 | 1 | 211596976 | regulatory region variant | T/C | snv | 0.86 | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||
|
1 | 1.000 | 15 | 26799458 | intron variant | A/C | snv | 0.59 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
|
1 | 1.000 | 1 | 18657203 | intron variant | G/A;T | snv | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 1.000 | 5 | 69129872 | 3 prime UTR variant | A/C;G | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
|
1 | 1.000 | 13 | 111997186 | intergenic variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||||
|
1 | 1.000 | 19 | 49782722 | splice region variant | C/T | snv | 9.3E-05 | 3.5E-05 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
1 | 1.000 | 6 | 10406842 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
1 | 1.000 | 2 | 120989858 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
1 | 1.000 | 15 | 45528960 | intron variant | G/A;T | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
|
1 | 1.000 | 16 | 84849496 | synonymous variant | C/T | snv | 4.0E-06; 0.70 | 0.61 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
1 | 1.000 | 13 | 104826293 | intergenic variant | C/T | snv | 0.38 | 0.010 | 1.000 | 1 | 2006 | 2006 | |||||
|
1 | 1.000 | 15 | 26712093 | intron variant | G/A | snv | 0.32 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
|
1 | 1.000 | 17 | 46824083 | intron variant | G/A | snv | 0.63 | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||
|
2 | 0.925 | 0.080 | 15 | 32758222 | intergenic variant | C/T | snv | 0.60 | 0.010 | 1.000 | 1 | 2018 | 2018 |