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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
14 | 0.763 | 0.240 | 11 | 1219991 | splice region variant | G/A;T | snv | 0.050 | 1.000 | 5 | 2013 | 2019 | |||||
|
10 | 0.790 | 0.080 | 8 | 22163096 | missense variant | T/A;C | snv | 3.6E-05 | 0.040 | 1.000 | 4 | 2004 | 2019 | ||||
|
10 | 0.790 | 0.240 | 16 | 2317763 | missense variant | T/A;C | snv | 2.3E-03 | 0.020 | 1.000 | 2 | 2012 | 2018 | ||||
|
83 | 0.550 | 0.880 | 5 | 1286401 | 3 prime UTR variant | C/A | snv | 0.52 | 0.810 | 1.000 | 2 | 2013 | 2014 | ||||
|
2 | 1.000 | 0.040 | 11 | 1100037 | intron variant | C/G;T | snv | 0.810 | 1.000 | 2 | 2013 | 2016 | |||||
|
1 | 15 | 40421575 | intron variant | A/G | snv | 0.45 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
53 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 15 | 40359637 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1 | 11 | 1325572 | intergenic variant | T/A;C;G | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1 | 6 | 7558085 | intron variant | T/C | snv | 0.20 | 0.21 | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
10 | 0.776 | 0.320 | 13 | 30737959 | intron variant | A/T | snv | 0.52 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 11 | 1062990 | intergenic variant | A/G | snv | 0.41 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
8 | 0.827 | 0.240 | 9 | 4292083 | intron variant | G/A | snv | 0.45 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 11 | 1061718 | intergenic variant | G/T | snv | 0.32 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 11 | 1061781 | intergenic variant | C/T | snv | 0.32 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 11 | 1062867 | intergenic variant | C/T | snv | 0.30 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 11 | 1067011 | intergenic variant | G/A | snv | 0.34 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 11 | 1060934 | TF binding site variant | C/A | snv | 0.31 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
2 | 1.000 | 0.040 | 11 | 1090036 | non coding transcript exon variant | T/C | snv | 0.73 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
32 | 0.637 | 0.600 | 3 | 169774313 | synonymous variant | C/T | snv | 0.29 | 0.21 | 0.700 | 1.000 | 1 | 2013 | 2013 | |||
|
2 | 1.000 | 0.160 | 3 | 169810661 | intron variant | C/T | snv | 0.37 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 11 | 1354730 | intron variant | C/T | snv | 0.54 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 15 | 40416223 | intron variant | A/G | snv | 0.68 | 0.61 | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
1 | 15 | 40433064 | intron variant | A/G | snv | 0.61 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
3 | 0.925 | 0.160 | 10 | 103913084 | intron variant | G/A | snv | 0.44 | 0.800 | 1.000 | 1 | 2013 | 2013 |