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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
17 | 0.851 | 0.160 | 11 | 61803876 | 5 prime UTR variant | C/G;T | snv | 0.700 | 1.000 | 3 | 2008 | 2013 | |||||
|
5 | 1.000 | 0.080 | 11 | 61801834 | 3 prime UTR variant | C/A;G | snv | 0.28 | 0.700 | 1.000 | 2 | 2012 | 2013 | ||||
|
17 | 0.807 | 0.200 | 11 | 61802358 | 3 prime UTR variant | C/T | snv | 0.28 | 0.700 | 1.000 | 2 | 2012 | 2013 | ||||
|
33 | 0.742 | 0.240 | 11 | 61803311 | intron variant | T/C | snv | 0.28 | 0.700 | 1.000 | 2 | 2010 | 2013 | ||||
|
12 | 0.851 | 0.240 | 11 | 61803910 | 5 prime UTR variant | G/A | snv | 0.26 | 0.700 | 1.000 | 2 | 2012 | 2013 | ||||
|
13 | 0.925 | 0.160 | 11 | 61804006 | 5 prime UTR variant | T/C | snv | 0.28 | 0.700 | 1.000 | 2 | 2012 | 2013 | ||||
|
4 | 11 | 61812288 | intron variant | T/C | snv | 0.26 | 0.700 | 1.000 | 2 | 2012 | 2013 | ||||||
|
7 | 0.925 | 0.160 | 11 | 61813163 | intron variant | C/T | snv | 0.26 | 0.700 | 1.000 | 2 | 2012 | 2013 | ||||
|
2 | 11 | 61800281 | 3 prime UTR variant | C/A | snv | 0.25 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 1.000 | 0.040 | 11 | 61807686 | intron variant | A/G;T | snv | 0.28 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
7 | 1.000 | 0.080 | 11 | 61811991 | intron variant | A/G | snv | 0.40 | 0.28 | 0.700 | 1.000 | 1 | 2012 | 2012 | |||
|
3 | 11 | 61814184 | non coding transcript exon variant | G/A | snv | 0.23 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
5 | 1.000 | 0.080 | 11 | 61814292 | non coding transcript exon variant | T/C | snv | 0.30 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
3 | 1.000 | 0.080 | 11 | 61815236 | 5 prime UTR variant | T/C | snv | 0.31 | 0.26 | 0.700 | 1.000 | 1 | 2012 | 2012 | |||
|
3 | 1.000 | 0.080 | 11 | 61817672 | intron variant | A/G | snv | 0.28 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
8 | 0.925 | 0.160 | 11 | 61824890 | intron variant | A/G | snv | 0.34 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
4 | 1.000 | 0.080 | 11 | 61826344 | missense variant | C/A;T | snv | 0.37 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
1 | 11 | 61819414 | intron variant | C/T | snv | 7.1E-02 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
7 | 0.851 | 0.240 | 11 | 61828092 | intron variant | C/T | snv | 0.11 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||
|
3 | 1.000 | 0.080 | 11 | 61829161 | intron variant | C/T | snv | 0.38 | 0.700 | 1.000 | 1 | 2012 | 2012 |