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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
9 | 0.776 | 0.320 | 22 | 41925447 | missense variant | G/A | snv | 5.7E-03 | 5.7E-03 | 0.010 | 1.000 | 1 | 2015 | 2015 | |||
|
7 | 0.851 | 0.120 | 12 | 6601978 | missense variant | A/C;G | snv | 2.0E-05; 1.2E-04; 5.2E-03 | 1.7E-03 | 0.010 | 1.000 | 1 | 2015 | 2015 | |||
|
6 | 0.851 | 0.240 | 4 | 73740952 | intron variant | T/G | snv | 0.45 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
3 | 0.925 | 0.120 | 1 | 207766701 | intron variant | G/T | snv | 0.46 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
64 | 0.566 | 0.800 | 4 | 73740307 | upstream gene variant | A/T | snv | 0.46 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
6 | 17 | 7675109 | missense variant | T/C | snv | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1 | 11 | 58292720 | non coding transcript exon variant | C/T | snv | 0.28 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||||
|
188 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||
|
52 | 0.597 | 0.560 | 13 | 102875652 | missense variant | G/C | snv | 0.28 | 0.30 | 0.010 | < 0.001 | 1 | 2013 | 2013 | |||
|
19 | 0.701 | 0.360 | 9 | 97697296 | 5 prime UTR variant | T/C;G | snv | 0.63; 4.5E-06; 4.5E-06 | 0.010 | < 0.001 | 1 | 2013 | 2013 | ||||
|
4 | 0.882 | 0.280 | 6 | 32774091 | intergenic variant | T/C | snv | 0.26 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 6 | 32700323 | TF binding site variant | G/A | snv | 0.27 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 8 | 131467654 | intergenic variant | C/T | snv | 0.43 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 6 | 32614112 | intergenic variant | C/T | snv | 0.10 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||||
|
2 | 1.000 | 0.120 | 3 | 187931631 | downstream gene variant | T/C | snv | 0.23 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||
|
3 | 0.925 | 0.120 | 6 | 14636732 | intergenic variant | T/C | snv | 0.74 | 0.810 | 1.000 | 1 | 2013 | 2013 | ||||
|
3 | 0.925 | 0.120 | 13 | 102872275 | missense variant | G/A | snv | 4.0E-06 | 4.9E-05 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||
|
3 | 0.925 | 0.120 | 20 | 63695147 | missense variant | G/A;T | snv | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
|
10 | 0.790 | 0.440 | 6 | 32461866 | intron variant | T/C | snv | 0.29 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 11 | 58580292 | intron variant | A/G | snv | 0.15 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||||
|
3 | 0.925 | 0.120 | 7 | 148809375 | missense variant | G/C | snv | 0.710 | 1.000 | 2 | 2012 | 2012 | |||||
|
242 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
214 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||
|
27 | 0.701 | 0.360 | 12 | 57751648 | missense variant | G/A;T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
7 | 0.925 | 0.160 | 7 | 148811636 | missense variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 |