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 | 159436169 | intron variant | T/C;G | snv | 0.700 | 1.000 | 2 | 2007 | 2012 | |||||||
|
1 | 1 | 159406553 | intron variant | A/G | snv | 0.10 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 1 | 159406562 | intron variant | C/A | snv | 0.10 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 1 | 159406113 | non coding transcript exon variant | C/T | snv | 0.11 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 1 | 159408804 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
2 | 1 | 159421611 | intron variant | G/A | snv | 0.47 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 1 | 159430569 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1 | 1 | 159431866 | intron variant | G/T | snv | 0.11 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 1 | 159433899 | intron variant | G/T | snv | 0.63 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 1 | 159415154 | intron variant | T/C | snv | 0.46 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 1 | 159440067 | missense variant | A/G | snv | 0.56 | 0.57 | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||
|
1 | 1 | 159427151 | intron variant | C/T | snv | 0.14 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 1 | 159440094 | missense variant | G/A | snv | 0.14 | 0.11 | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||
|
1 | 1 | 159439689 | intron variant | T/A;G | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1 | 1 | 159407668 | intron variant | T/C | snv | 0.37 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 1 | 159422073 | intron variant | T/C | snv | 0.11 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 1 | 159441185 | 3 prime UTR variant | G/A | snv | 0.18 | 0.700 | 1.000 | 1 | 2012 | 2012 |