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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
29 | 0.653 | 0.440 | 2 | 43839108 | missense variant | G/A;C | snv | 6.4E-06; 6.7E-02 | 0.800 | 1.000 | 11 | 2007 | 2018 | ||||
|
2 | 0.925 | 0.040 | 8 | 46473341 | intergenic variant | A/G | snv | 9.8E-03 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 2 | 159382207 | intron variant | A/G | snv | 2.5E-02 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 8 | 15004905 | intron variant | C/A;G | snv | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||
|
2 | 0.925 | 0.040 | 10 | 68210229 | intron variant | C/T | snv | 0.26 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 10 | 80580951 | intron variant | T/C | snv | 8.6E-02 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 12 | 85855418 | intergenic variant | T/C | snv | 0.37 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 11 | 76739864 | intergenic variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||
|
2 | 0.925 | 0.040 | 22 | 49583909 | intron variant | A/C | snv | 4.4E-02 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 20 | 60093953 | intron variant | A/G | snv | 0.23 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 1 | 185895380 | intron variant | A/G | snv | 7.6E-02 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 2 | 159061866 | intron variant | T/C | snv | 1.2E-02 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 9 | 77424742 | intron variant | A/G | snv | 7.2E-02 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 18 | 59981043 | intergenic variant | T/C | snv | 3.3E-02 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 13 | 71683104 | intron variant | T/C | snv | 8.5E-02 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 9 | 115062806 | intron variant | G/A | snv | 0.11 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 19 | 52827416 | intron variant | C/T | snv | 0.11 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
4 | 0.851 | 0.080 | 12 | 114991548 | intergenic variant | T/C | snv | 0.21 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 5 | 16871155 | intron variant | A/C | snv | 6.9E-02 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 7 | 67861752 | intergenic variant | C/A | snv | 0.89 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
3 | 0.882 | 0.080 | 2 | 43846517 | non coding transcript exon variant | T/C | snv | 7.9E-02 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 9 | 122717961 | intergenic variant | G/A | snv | 7.9E-02 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 10 | 13834687 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||
|
8 | 0.882 | 0.080 | 2 | 43847292 | non coding transcript exon variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||
|
11 | 0.851 | 0.120 | 2 | 43845437 | intron variant | G/C;T | snv | 0.700 | 1.000 | 1 | 2007 | 2007 |