| 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. | ||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
15 | 0.716 | 0.320 | 15 | 73927241 | missense variant | G/A;C;T | snv | 0.18; 4.5E-06 | 0.900 | 0.955 | 44 | 2007 | 2019 | ||||
|
1 | 1.000 | 0.040 | 15 | 73936854 | intron variant | G/A | snv | 0.29 | 0.810 | 1.000 | 2 | 2014 | 2019 | ||||
|
15 | 0.716 | 0.360 | 15 | 73929861 | intron variant | T/C | snv | 0.60 | 0.800 | 1.000 | 23 | 2008 | 2019 | ||||
|
1 | 1.000 | 0.040 | 15 | 73951556 | intron variant | G/A | snv | 5.6E-02 | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||
|
1 | 1.000 | 0.040 | 15 | 73934799 | intron variant | A/T | snv | 8.4E-02 | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||
|
1 | 1.000 | 0.040 | 15 | 73928957 | intron variant | C/T | snv | 0.31 | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||
|
1 | 1.000 | 0.040 | 15 | 73939008 | intron variant | C/T | snv | 3.6E-02 | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||
|
2 | 0.925 | 0.040 | 15 | 73931426 | intron variant | C/G | snv | 0.29 | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||
|
1 | 1.000 | 0.040 | 15 | 73932655 | intron variant | G/A | snv | 0.28 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
1 | 1.000 | 0.040 | 15 | 73936123 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||
|
1 | 1.000 | 0.040 | 15 | 73948894 | intron variant | T/C | snv | 0.23 | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||
|
14 | 0.732 | 0.320 | 15 | 73927205 | missense variant | G/T | snv | 0.33 | 0.28 | 0.100 | 0.892 | 37 | 2008 | 2019 | |||
|
2 | 0.925 | 0.040 | 15 | 73927743 | synonymous variant | G/T | snv | 6.1E-02 | 3.7E-02 | 0.020 | 1.000 | 2 | 2013 | 2019 | |||
|
2 | 0.925 | 0.040 | 15 | 73926125 | 5 prime UTR variant | A/C | snv | 0.33 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
1 | 1.000 | 0.040 | 15 | 73952003 | 3 prime UTR variant | C/T | snv | 0.48 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
1 | 1.000 | 0.040 | 15 | 73952269 | downstream gene variant | A/G;T | snv | 0.010 | 1.000 | 1 | 2019 | 2019 |