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 | 0.925 | 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 | 2 | 43873860 | missense variant | A/C;G | snv | 8.0E-06; 3.8E-04 | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||
|
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 | ||||
|
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 | ||||
|
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 | |||||
|
2 | 0.925 | 0.040 | 1 | 27779198 | intron variant | T/C | snv | 0.18 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 22 | 23680444 | intron variant | C/T | snv | 0.49 | 0.700 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.040 | 2 | 43852775 | missense variant | C/T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
2 | 0.925 | 0.040 | 16 | 8540871 | intron variant | G/A | snv | 0.11 | 0.700 | 1.000 | 1 | 2007 | 2007 |