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 | 10 | 76131488 | intron variant | T/G | snv | 0.16 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 1 | 51080468 | intergenic variant | T/G | snv | 3.7E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
3 | 1.000 | 0.080 | 3 | 12800724 | intron variant | T/G | snv | 0.63 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
2 | 2 | 36446412 | intron variant | T/G | snv | 0.48 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 1 | 61408005 | intron variant | T/G | snv | 0.44 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
4 | 6 | 118346359 | intergenic variant | T/C | snv | 0.40 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 21 | 28781917 | regulatory region variant | T/C | snv | 8.7E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 2 | 37020872 | intron variant | T/C | snv | 0.24 | 0.18 | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
8 | 1.000 | 0.040 | 17 | 46935905 | 3 prime UTR variant | T/C | snv | 9.2E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
1 | 2 | 174603041 | intron variant | T/C | snv | 0.79 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 1 | 115768346 | missense variant | T/C | snv | 0.33 | 0.34 | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
7 | 1.000 | 0.080 | 3 | 38725824 | intron variant | T/C | snv | 0.67 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
1 | 12 | 114943266 | intergenic variant | T/C | snv | 0.27 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 6 | 7502516 | upstream gene variant | T/C | snv | 5.4E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 10 | 18406963 | intron variant | T/C | snv | 0.44 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 16 | 11595035 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
2 | 13 | 73946049 | intron variant | T/A | snv | 0.40 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 14 | 71417850 | intron variant | G/T | snv | 0.18 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 6 | 159472905 | intron variant | G/T | snv | 0.31 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 10 | 112719503 | intron variant | G/C;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
6 | 0.925 | 0.120 | 3 | 38592432 | intron variant | G/C | snv | 0.11 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
1 | 18 | 36731696 | intron variant | G/C | snv | 0.40 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 1 | 61432295 | intron variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
12 | 0.776 | 0.080 | 6 | 36655602 | regulatory region variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
1 | 4 | 20182314 | intergenic variant | G/A;C;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 |