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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 1.000 | 0.160 | X | 67722881 | missense variant | A/G | snv | 0.700 | 1.000 | 20 | 1992 | 2004 | |||||
|
2 | 0.925 | 0.160 | X | 67717552 | missense variant | A/G | snv | 0.700 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 1.000 | 0.160 | X | 67721881 | missense variant | G/T | snv | 5.5E-06 | 0.700 | 1.000 | 20 | 1992 | 2004 | ||||
|
1 | 1.000 | 0.160 | X | 67546480 | missense variant | A/G | snv | 1.8E-05 | 1.0E-05 | 0.700 | 1.000 | 20 | 1992 | 2004 | |||
|
1 | 0.925 | 0.160 | X | 67721837 | missense variant | C/T | snv | 0.800 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 1.000 | 0.160 | X | 67721876 | missense variant | A/G | snv | 0.800 | 1.000 | 20 | 1992 | 2004 | |||||
|
2 | 0.925 | 0.160 | X | 67721838 | missense variant | G/A | snv | 0.800 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 1.000 | 0.160 | X | 67711549 | missense variant | T/C | snv | 0.800 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 1.000 | 0.160 | X | 67711639 | missense variant | T/G | snv | 0.800 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 1.000 | 0.160 | X | 67643378 | missense variant | G/A;T | snv | 0.810 | 1.000 | 20 | 1992 | 2005 | |||||
|
1 | 0.925 | 0.160 | X | 67643284 | missense variant | C/T | snv | 0.700 | 1.000 | 20 | 1992 | 2004 | |||||
|
2 | 0.925 | 0.160 | X | 67721857 | missense variant | G/A;T | snv | 5.5E-06 | 0.800 | 1.000 | 20 | 1992 | 2004 | ||||
|
1 | 1.000 | 0.160 | X | 67722973 | missense variant | T/C | snv | 0.800 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 1.000 | 0.160 | X | 67722948 | missense variant | C/G;T | snv | 5.5E-06 | 0.800 | 1.000 | 20 | 1992 | 2004 | ||||
|
2 | 0.925 | 0.160 | X | 67717535 | missense variant | G/A;T | snv | 0.810 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 1.000 | 0.160 | X | 67686091 | missense variant | T/C | snv | 0.800 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 1.000 | 0.160 | X | 67711560 | missense variant | G/A | snv | 0.800 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 1.000 | 0.160 | X | 67711602 | missense variant | G/A | snv | 0.800 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 1.000 | 0.160 | X | 67711620 | missense variant | C/T | snv | 0.800 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 1.000 | 0.160 | X | 67721951 | missense variant | C/T | snv | 0.710 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 1.000 | 0.160 | X | 67722970 | missense variant | G/A | snv | 0.800 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 1.000 | 0.160 | X | 67723774 | missense variant | T/C | snv | 0.700 | 1.000 | 20 | 1992 | 2004 | |||||
|
1 | 0.925 | 0.160 | X | 67546320 | missense variant | C/T | snv | 4.5E-03 | 2.0E-03 | 0.700 | 1.000 | 20 | 1992 | 2004 | |||
|
2 | 0.925 | 0.160 | X | 67686088 | missense variant | G/A | snv | 5.5E-06 | 0.800 | 1.000 | 20 | 1992 | 2004 | ||||
|
1 | 1.000 | 0.160 | X | 67723737 | missense variant | A/G;T | snv | 1.3E-04; 5.5E-06 | 0.700 | 1.000 | 20 | 1992 | 2004 |