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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
38 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 0.800 | 1.000 | 7 | 2010 | 2019 | ||||
|
5 | 16 | 88787321 | upstream gene variant | C/G;T | snv | 0.800 | 1.000 | 5 | 2010 | 2019 | |||||||
|
13 | 6 | 135097778 | intron variant | A/G | snv | 0.24 | 0.800 | 1.000 | 4 | 2012 | 2018 | ||||||
|
226 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.800 | 1.000 | 3 | 2012 | 2018 | |||
|
6 | 22 | 37074184 | intron variant | T/C | snv | 0.61 | 0.800 | 1.000 | 3 | 2012 | 2017 | ||||||
|
12 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 0.800 | 1.000 | 3 | 2012 | 2018 | |||||
|
14 | 0.851 | 0.160 | 22 | 37073551 | missense variant | G/A;C | snv | 0.53; 4.0E-06 | 0.800 | 1.000 | 3 | 2010 | 2019 | ||||
|
1 | 8 | 42602307 | intergenic variant | T/C | snv | 0.69 | 0.800 | 1.000 | 3 | 2012 | 2019 | ||||||
|
2 | 11 | 5209677 | downstream gene variant | T/C | snv | 3.5E-02 | 0.800 | 1.000 | 3 | 2013 | 2019 | ||||||
|
14 | 1.000 | 0.080 | 6 | 135097497 | intron variant | C/T | snv | 6.9E-02 | 0.800 | 1.000 | 3 | 2010 | 2012 | ||||
|
3 | 16 | 264781 | intron variant | G/A;T | snv | 2.9E-05; 6.5E-03 | 0.800 | 1.000 | 3 | 2013 | 2019 | ||||||
|
1 | 16 | 88774054 | intron variant | G/A | snv | 0.49 | 0.800 | 1.000 | 2 | 2012 | 2019 | ||||||
|
15 | 0.790 | 0.200 | X | 154536002 | missense variant | C/T | snv | 9.1E-03 | 3.6E-02 | 0.700 | 1.000 | 2 | 2013 | 2013 | |||
|
1 | 18 | 46139716 | intergenic variant | G/A;C | snv | 0.800 | 1.000 | 2 | 2012 | 2016 | |||||||
|
4 | 19 | 12890733 | upstream gene variant | A/G | snv | 0.31 | 0.800 | 1.000 | 2 | 2012 | 2016 | ||||||
|
2 | 16 | 259156 | intron variant | C/A | snv | 0.19 | 0.800 | 1.000 | 2 | 2012 | 2013 | ||||||
|
5 | 1 | 3774964 | intron variant | A/G | snv | 0.31 | 0.800 | 1.000 | 2 | 2012 | 2016 | ||||||
|
1 | 3 | 196089324 | intergenic variant | C/T | snv | 0.42 | 0.800 | 1.000 | 2 | 2012 | 2016 | ||||||
|
5 | 2 | 46128709 | intron variant | C/A | snv | 0.10 | 0.700 | 1.000 | 2 | 2012 | 2013 | ||||||
|
3 | 6 | 30160096 | intron variant | C/T | snv | 0.11 | 0.800 | 1.000 | 2 | 2012 | 2016 | ||||||
|
4 | 16 | 260381 | intron variant | G/A;C | snv | 1.1E-02 | 0.800 | 1.000 | 2 | 2013 | 2019 | ||||||
|
5 | 16 | 248589 | intron variant | A/G | snv | 3.8E-02 | 0.800 | 1.000 | 2 | 2013 | 2017 | ||||||
|
2 | 1 | 203682799 | 5 prime UTR variant | T/A;C | snv | 0.800 | 1.000 | 2 | 2012 | 2013 | |||||||
|
8 | 6 | 25821542 | intron variant | C/T | snv | 6.1E-02 | 0.700 | 1.000 | 2 | 2010 | 2012 | ||||||
|
262 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 0.700 | 1.000 | 2 | 2010 | 2012 |