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 | 9 | 22084311 | intron variant | C/T | snv | 0.55 | 0.800 | 1.000 | 3 | 2011 | 2013 | |||||
|
2 | 9 | 22112600 | intron variant | T/A;C | snv | 0.700 | 1.000 | 2 | 2011 | 2013 | |||||||
|
2 | 9 | 22106732 | intron variant | T/A | snv | 0.64 | 0.700 | 1.000 | 2 | 2011 | 2013 | ||||||
|
1 | 9 | 22099569 | intron variant | C/A;T | snv | 0.700 | 1.000 | 2 | 2011 | 2013 | |||||||
|
1 | 9 | 22100177 | intron variant | G/A;C | snv | 0.700 | 1.000 | 2 | 2011 | 2013 | |||||||
|
2 | 9 | 22112242 | intron variant | A/C | snv | 0.65 | 0.700 | 1.000 | 2 | 2011 | 2013 | ||||||
|
1 | 9 | 22125914 | intron variant | C/T | snv | 0.50 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||
|
1 | 9 | 22029058 | intron variant | T/A | snv | 2.1E-05 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 9 | 22029059 | intron variant | AA/-;A;AAA;AAAA | delins | 6.9E-03 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 9 | 22029059 | intron variant | AA/-;A;AAA;AAAA | delins | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1 | 9 | 22029059 | intron variant | AA/-;A;AAA;AAAA | delins | 0.58 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 9 | 22071751 | intron variant | C/T | snv | 0.69 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 9 | 22029059 | intron variant | AA/-;A;AAA;AAAA | delins | 8.0E-04 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 9 | 22112428 | intron variant | A/G | snv | 0.65 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 9 | 22124141 | intron variant | A/T | snv | 0.64 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
2 | 9 | 22105928 | intron variant | T/C | snv | 0.64 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||
|
2 | 1.000 | 0.040 | 9 | 22115590 | intron variant | A/C;T | snv | 0.700 | 1.000 | 2 | 2011 | 2013 | |||||
|
3 | 1.000 | 0.040 | 9 | 22114496 | intron variant | A/C;G;T | snv | 0.700 | 1.000 | 2 | 2011 | 2013 | |||||
|
3 | 1.000 | 0.040 | 9 | 22072265 | intron variant | A/C;G | snv | 0.700 | 1.000 | 2 | 2011 | 2013 | |||||
|
3 | 1.000 | 0.040 | 9 | 22065003 | intron variant | C/G;T | snv | 0.700 | 1.000 | 2 | 2011 | 2013 | |||||
|
2 | 1.000 | 0.040 | 9 | 22067831 | intron variant | G/A;C | snv | 0.700 | 1.000 | 2 | 2011 | 2013 | |||||
|
2 | 1.000 | 0.040 | 9 | 22067277 | intron variant | T/A | snv | 0.64 | 0.700 | 1.000 | 2 | 2011 | 2013 | ||||
|
2 | 1.000 | 0.040 | 9 | 22065658 | splice region variant | G/A;C;T | snv | 0.700 | 1.000 | 2 | 2011 | 2013 | |||||
|
2 | 1.000 | 0.040 | 9 | 22116047 | intron variant | A/G | snv | 0.64 | 0.700 | 1.000 | 2 | 2011 | 2013 | ||||
|
2 | 1.000 | 0.040 | 9 | 22036368 | non coding transcript exon variant | C/T | snv | 0.71 | 0.700 | 1.000 | 2 | 2011 | 2013 |