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 | 20 | 33410203 | missense variant | G/A | snv | 2.0E-05 | 1.4E-05 | 0.700 | 0 | ||||||
|
2 | 0.925 | 0.120 | 3 | 38555720 | missense variant | T/C | snv | 1.6E-05 | 3.5E-05 | 0.700 | 0 | ||||||
|
5 | 0.827 | 0.120 | 7 | 151560611 | missense variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2001 | 2001 | |||||
|
5 | 0.882 | 0.160 | 1 | 156130741 | missense variant | G/A | snv | 0.010 | 1.000 | 1 | 2003 | 2003 | |||||
|
11 | 0.776 | 0.200 | 1 | 156136094 | missense variant | G/A;T | snv | 0.010 | 1.000 | 1 | 2003 | 2003 | |||||
|
106 | 0.532 | 0.760 | 12 | 6845711 | synonymous variant | C/T | snv | 0.36 | 0.44 | 0.010 | 1.000 | 1 | 2004 | 2004 | |||
|
1 | 1.000 | 0.080 | 7 | 150955422 | missense variant | G/A;C | snv | 7.1E-05 | 4.2E-05 | 0.010 | 1.000 | 1 | 2004 | 2004 | |||
|
3 | 0.882 | 0.120 | 21 | 34370557 | missense variant | C/A;T | snv | 4.0E-06; 1.3E-04 | 0.010 | 1.000 | 1 | 2004 | 2004 | ||||
|
3 | 0.882 | 0.080 | 11 | 99622442 | intron variant | C/G | snv | 0.14 | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||
|
614 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 0.010 | 1.000 | 1 | 2007 | 2007 | |||
|
135 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 0.010 | 1.000 | 1 | 2007 | 2007 | |||
|
10 | 0.776 | 0.160 | 21 | 34449382 | missense variant | C/T | snv | 9.4E-03 | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||
|
1 | 1.000 | 0.080 | 11 | 2527981 | missense variant | A/G | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 1.000 | 0.080 | 11 | 2445138 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||
|
4 | 0.851 | 0.080 | 16 | 79516830 | downstream gene variant | C/A;T | snv | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||
|
22 | 0.708 | 0.400 | 7 | 150998541 | missense variant | C/T | snv | 4.1E-06 | 4.2E-05 | 0.010 | 1.000 | 1 | 2007 | 2007 | |||
|
4 | 0.851 | 0.080 | 6 | 13332235 | upstream gene variant | G/A | snv | 0.21 | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||
|
5 | 0.851 | 0.080 | 10 | 116816095 | intron variant | G/A | snv | 0.40 | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.120 | 3 | 38550748 | missense variant | A/G;T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||
|
2 | 0.925 | 0.080 | 5 | 37341164 | missense variant | C/T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||
|
5 | 0.851 | 0.240 | 1 | 156130688 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2008 | 2008 | |||||
|
1 | 1.000 | 0.080 | 4 | 110807458 | intergenic variant | A/G | snv | 0.47 | 0.700 | 1.000 | 2 | 2007 | 2009 | ||||
|
1 | 1.000 | 0.080 | 4 | 110719897 | intergenic variant | A/G | snv | 0.37 | 0.700 | 1.000 | 2 | 2007 | 2009 | ||||
|
3 | 0.925 | 0.080 | 17 | 70175316 | missense variant | G/A | snv | 1.6E-04 | 7.0E-05 | 0.020 | 1.000 | 2 | 2005 | 2009 | |||
|
1 | 1.000 | 0.080 | 12 | 5045727 | missense variant | C/T | snv | 1.4E-04 | 4.9E-05 | 0.010 | 1.000 | 1 | 2009 | 2009 |