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 | 1.000 | 0.040 | 9 | 22121350 | intron variant | A/T | snv | 0.52 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
3 | 1.000 | 0.040 | 9 | 22025494 | intron variant | G/A | snv | 0.29 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||
|
3 | 0.925 | 0.120 | 9 | 22049131 | non coding transcript exon variant | C/A;G | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
2 | 1.000 | 0.040 | 9 | 22088091 | intron variant | A/T | snv | 0.42 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
2 | 1.000 | 0.040 | 9 | 22019733 | intron variant | A/G | snv | 0.58 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
2 | 1.000 | 0.040 | 9 | 22048860 | intron variant | T/C | snv | 0.49 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
2 | 1.000 | 0.040 | 9 | 22052811 | intron variant | G/A;C;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
2 | 1.000 | 0.040 | 9 | 22072720 | intron variant | A/C;G | snv | 0.40 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
2 | 1.000 | 0.040 | 9 | 22124451 | intron variant | A/G | snv | 0.40 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
3 | 0.925 | 0.040 | 9 | 22124631 | intron variant | A/G | snv | 0.40 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
2 | 1.000 | 0.040 | 9 | 22014138 | non coding transcript exon variant | C/G | snv | 0.32 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||
|
2 | 1.000 | 0.040 | 9 | 22024967 | intron variant | A/G | snv | 0.56 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
2 | 1.000 | 0.040 | 9 | 22049657 | intron variant | G/A | snv | 0.59 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
7 | 0.807 | 0.200 | 9 | 22124473 | intron variant | C/T | snv | 0.47 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
3 | 0.925 | 0.080 | 9 | 22023796 | intron variant | T/A;C;G | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
4 | 0.882 | 0.120 | 9 | 22029446 | missense variant | G/A | snv | 0.55 | 0.46 | 0.700 | 1.000 | 1 | 2013 | 2013 | |||
|
4 | 0.882 | 0.080 | 9 | 22053688 | intron variant | A/G | snv | 0.58 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
2 | 1.000 | 0.040 | 9 | 22043820 | intron variant | T/C | snv | 0.58 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
3 | 0.925 | 0.040 | 9 | 22040766 | intron variant | C/T | snv | 0.71 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||
|
15 | 0.732 | 0.280 | 9 | 22083405 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||
|
14 | 0.776 | 0.280 | 9 | 22119196 | non coding transcript exon variant | T/C | snv | 0.50 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||
|
1 | 9 | 22125914 | intron variant | C/T | snv | 0.50 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||
|
2 | 1.000 | 0.040 | 9 | 22045318 | intron variant | C/T | snv | 0.72 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||
|
2 | 1.000 | 0.040 | 9 | 22041444 | intron variant | T/C;G | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
14 | 0.742 | 0.400 | 9 | 22043927 | intron variant | A/G | snv | 0.28 | 0.700 | 1.000 | 1 | 2011 | 2011 |