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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
33 | 0.662 | 0.320 | 6 | 160589086 | intron variant | A/G | snv | 4.3E-02 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
1 | 5 | 35044193 | intron variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
54 | 0.597 | 0.640 | 5 | 148826910 | stop gained | G/C;T | snv | 0.68 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
8 | 1.000 | 0.160 | 16 | 16182534 | stop gained | C/A;T | snv | 9.1E-05 | 4.2E-05 | 0.700 | 0 | ||||||
|
4 | 1.000 | 0.160 | 16 | 16157755 | stop gained | G/A | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
7 | 0.925 | 0.200 | 16 | 16173393 | stop gained | G/C;T | snv | 4.0E-06 | 7.0E-06 | 0.700 | 0 | ||||||
|
7 | 0.882 | 0.240 | 16 | 16154644 | stop gained | G/A | snv | 2.0E-05 | 7.0E-06 | 0.700 | 0 | ||||||
|
12 | 0.851 | 0.280 | 16 | 16202045 | stop gained | G/A | snv | 4.8E-05 | 1.8E-04 | 0.700 | 0 | ||||||
|
12 | 0.827 | 0.240 | 16 | 16190247 | stop gained | G/A;T | snv | 4.4E-05; 4.0E-06 | 0.700 | 0 | |||||||
|
4 | 1.000 | 0.160 | 16 | 16169827 | stop gained | G/C;T | snv | 0.700 | 0 | ||||||||
|
32 | 0.695 | 0.480 | 16 | 16163078 | stop gained | G/A | snv | 1.4E-03 | 1.2E-03 | 0.700 | 0 | ||||||
|
14 | 0.807 | 0.320 | 16 | 16163009 | stop gained | G/A | snv | 1.7E-04 | 1.2E-04 | 0.700 | 0 | ||||||
|
5 | 1.000 | 0.160 | 16 | 16219655 | stop gained | C/A;T | snv | 1.8E-05; 7.8E-04 | 0.700 | 0 | |||||||
|
63 | 0.576 | 0.800 | 5 | 148826877 | missense variant | G/A | snv | 0.42 | 0.43 | 0.010 | 1.000 | 1 | 2010 | 2010 | |||
|
3 | 0.925 | 0.200 | 16 | 16182506 | missense variant | T/C | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
5 | 1.000 | 0.160 | 16 | 16178955 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
5 | 1.000 | 0.160 | 16 | 16214428 | missense variant | G/A | snv | 4.6E-04 | 3.0E-04 | 0.700 | 0 | ||||||
|
12 | 0.827 | 0.240 | 16 | 16163087 | missense variant | G/A | snv | 4.4E-05 | 3.5E-05 | 0.700 | 0 | ||||||
|
13 | 0.851 | 0.320 | 16 | 16154899 | missense variant | G/A;T | snv | 8.2E-05 | 0.700 | 0 | |||||||
|
11 | 0.882 | 0.280 | 16 | 16163086 | missense variant | C/G;T | snv | 7.6E-05 | 0.700 | 0 | |||||||
|
7 | 0.925 | 0.160 | 16 | 16163159 | missense variant | G/A | snv | 9.2E-05 | 4.2E-05 | 0.700 | 0 | ||||||
|
9 | 0.925 | 0.200 | 16 | 16159505 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
11 | 0.851 | 0.200 | 16 | 16155010 | missense variant | C/T | snv | 4.8E-05 | 2.8E-05 | 0.700 | 0 | ||||||
|
4 | 1.000 | 0.160 | 16 | 16159541 | missense variant | G/T | snv | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.200 | 16 | 16163084 | missense variant | C/T | snv | 5.2E-05 | 2.8E-05 | 0.700 | 0 |