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 | 1 | 94030497 | missense variant | G/A | snv | 4.6E-03 | 1.6E-03 | 0.010 | 1.000 | 1 | 1999 | 1999 | |||
|
4 | 0.882 | 0.160 | 1 | 94042767 | missense variant | G/A | snv | 1.2E-04 | 1.8E-04 | 0.010 | 1.000 | 1 | 1999 | 1999 | |||
|
8 | 0.790 | 0.080 | 1 | 94098928 | missense variant | G/A;T | snv | 1.1E-04; 8.0E-06 | 0.010 | 1.000 | 1 | 1999 | 1999 | ||||
|
1 | 1.000 | 0.040 | 1 | 203499804 | missense variant | C/T | snv | 6.0E-05 | 7.7E-05 | 0.010 | 1.000 | 1 | 2002 | 2002 | |||
|
13 | 0.752 | 0.280 | 2 | 136115399 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 0.010 | 1.000 | 1 | 2004 | 2004 | ||||
|
56 | 0.592 | 0.760 | 1 | 225831932 | missense variant | T/C | snv | 0.32 | 0.27 | 0.010 | 1.000 | 1 | 2005 | 2005 | |||
|
1 | 1.000 | 0.040 | 6 | 159684905 | missense variant | G/A | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||
|
3 | 0.882 | 0.120 | 15 | 74750069 | frameshift variant | CT/- | delins | 4.0E-06 | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||
|
2 | 0.925 | 0.040 | 6 | 79916658 | missense variant | T/C | snv | 0.17 | 0.16 | 0.020 | 1.000 | 2 | 2005 | 2006 | |||
|
23 | 0.677 | 0.480 | 19 | 44908690 | missense variant | C/A;T | snv | 2.1E-05 | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||
|
3 | 0.882 | 0.120 | 14 | 91870336 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2006 | 2006 | |||||
|
1 | 1.000 | 0.040 | 6 | 43780784 | missense variant | C/A;T | snv | 4.0E-06; 2.8E-05 | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||
|
5 | 0.827 | 0.160 | 20 | 25077762 | missense variant | T/C;G | snv | 2.7E-03 | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||
|
6 | 0.827 | 0.200 | 6 | 43782077 | missense variant | C/G;T | snv | 8.0E-06 | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||
|
3 | 0.882 | 0.120 | 14 | 91887283 | missense variant | A/G | snv | 0.010 | 1.000 | 1 | 2006 | 2006 | |||||
|
3 | 0.925 | 0.040 | 1 | 186178506 | missense variant | A/G | snv | 7.3E-04 | 6.8E-04 | 0.050 | 1.000 | 5 | 2004 | 2007 | |||
|
1 | 1.000 | 0.040 | 7 | 33199222 | intron variant | A/G | snv | 0.19 | 0.010 | < 0.001 | 1 | 2007 | 2007 | ||||
|
3 | 0.882 | 0.120 | X | 97043550 | intron variant | G/A | snv | 0.41 | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||
|
3 | 0.882 | 0.120 | 6 | 43777370 | non coding transcript exon variant | G/A | snv | 0.31 | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||
|
4 | 0.851 | 0.160 | 10 | 122461760 | synonymous variant | G/C;T | snv | 5.9E-02; 0.32 | 0.020 | 1.000 | 2 | 2008 | 2008 | ||||
|
182 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 0.020 | 0.500 | 2 | 2005 | 2008 | |||
|
14 | 0.763 | 0.360 | X | 12885540 | missense variant | A/C;T | snv | 0.18 | 0.18 | 0.010 | 1.000 | 1 | 2008 | 2008 | |||
|
4 | 0.851 | 0.120 | 16 | 55493201 | synonymous variant | G/A;C | snv | 0.39; 8.0E-06 | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||
|
1 | 1.000 | 0.040 | 1 | 153974702 | missense variant | G/A;C | snv | 4.4E-05; 4.0E-06 | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||
|
2 | 0.925 | 0.160 | 2 | 209633537 | intron variant | G/A | snv | 0.30 | 0.010 | 1.000 | 1 | 2008 | 2008 |