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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
5 | 0.851 | 0.120 | 15 | 66435103 | missense variant | T/A;C;G | snv | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||
|
6 | 0.827 | 0.080 | 15 | 66435113 | missense variant | A/C | snv | 0.700 | 1.000 | 2 | 2009 | 2013 | |||||
|
2 | 1.000 | 0.040 | 15 | 66436786 | missense variant | T/A;G | snv | 0.700 | 1.000 | 2 | 2011 | 2012 | |||||
|
2 | 0.925 | 0.040 | 15 | 66436816 | missense variant | G/C | snv | 0.720 | 1.000 | 5 | 2011 | 2014 | |||||
|
6 | 0.827 | 0.160 | 15 | 66436824 | missense variant | C/A;T | snv | 0.700 | 1.000 | 3 | 2009 | 2012 | |||||
|
1 | 1.000 | 0.040 | 15 | 66481793 | missense variant | G/A | snv | 0.700 | 1.000 | 3 | 2009 | 2013 | |||||
|
1 | 1.000 | 0.040 | 15 | 66485086 | missense variant | C/T | snv | 0.700 | 1.000 | 2 | 2011 | 2012 | |||||
|
1 | 1.000 | 0.040 | 15 | 66490577 | missense variant | A/C | snv | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||
|
3 | 1.000 | 0.040 | 15 | 66436839 | missense variant | T/C | snv | 0.700 | 1.000 | 2 | 2009 | 2013 | |||||
|
2 | 0.925 | 0.040 | 15 | 66436815 | missense variant | T/A | snv | 0.020 | 1.000 | 2 | 2014 | 2014 | |||||
|
7 | 0.807 | 0.240 | 15 | 66436837 | missense variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
2 | 0.925 | 0.200 | 15 | 66435115 | missense variant | A/C;G | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
6 | 0.827 | 0.280 | 15 | 66436825 | missense variant | C/A;G;T | snv | 0.720 | 1.000 | 5 | 2009 | 2015 | |||||
|
6 | 0.807 | 0.320 | 15 | 66435145 | missense variant | G/A | snv | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
9 | 0.763 | 0.400 | 15 | 66435117 | missense variant | G/C;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 |