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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
4 | 0.827 | 0.040 | 3 | 186539566 | missense variant | C/A | snv | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
|
6 | 0.807 | 0.120 | 15 | 90811275 | synonymous variant | C/T | snv | 0.15 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
7 | 0.776 | 0.160 | 8 | 31119144 | intron variant | T/C | snv | 0.16 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 1.000 | 0.040 | 5 | 11108043 | intron variant | C/T | snv | 7.0E-02 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
1 | 1.000 | 0.040 | 5 | 11110237 | intron variant | C/A;T | snv | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||
|
1 | 1.000 | 0.040 | 5 | 11111141 | intron variant | T/G | snv | 7.6E-02 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
1 | 1.000 | 0.040 | 21 | 25971876 | intron variant | A/C | snv | 0.17 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
2 | 0.925 | 0.120 | 1 | 147909431 | downstream gene variant | A/G | snv | 0.17 | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||
|
7 | 0.790 | 0.120 | 8 | 31042501 | intron variant | G/A | snv | 7.6E-02 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
6 | 0.807 | 0.120 | 8 | 31075099 | intron variant | C/G | snv | 0.76 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
6 | 0.807 | 0.120 | 8 | 31043374 | intron variant | A/G | snv | 0.50 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
2 | 0.925 | 0.120 | 1 | 147905591 | upstream gene variant | G/T | snv | 0.27 | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||
|
1 | 1.000 | 0.040 | 1 | 16148628 | synonymous variant | C/G;T | snv | 0.30 | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||
|
2 | 0.925 | 0.120 | 1 | 147903855 | upstream gene variant | C/T | snv | 0.55 | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||
|
4 | 0.882 | 0.120 | 7 | 134431881 | intron variant | G/A | snv | 0.21 | 0.010 | < 0.001 | 1 | 2018 | 2018 |