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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
48 | 0.623 | 0.280 | 7 | 55191846 | missense variant | A/T | snv | 0.100 | 0.913 | 23 | 2008 | 2019 | |||||
|
8 | 0.790 | 0.120 | 7 | 55191837 | missense variant | G/A | snv | 0.040 | 1.000 | 4 | 2016 | 2019 | |||||
|
31 | 0.658 | 0.520 | 7 | 55161562 | missense variant | G/A;C;T | snv | 0.29 | 0.030 | 1.000 | 3 | 2007 | 2018 | ||||
|
5 | 0.851 | 0.080 | 7 | 55160316 | missense variant | C/A | snv | 0.020 | 1.000 | 2 | 2013 | 2019 | |||||
|
70 | 0.581 | 0.520 | 7 | 55181378 | missense variant | C/T | snv | 2.8E-05 | 5.6E-05 | 0.020 | 1.000 | 2 | 2018 | 2019 | |||
|
7 | 0.827 | 0.120 | 7 | 55019338 | missense variant | G/A;T | snv | 1.1E-04 | 0.020 | 1.000 | 2 | 2006 | 2007 | ||||
|
6 | 0.851 | 0.120 | 7 | 55181370 | missense variant | G/A;C | snv | 0.52; 4.0E-06 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
2 | 0.925 | 0.080 | 7 | 55143316 | missense variant | G/C | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.080 | 7 | 55200363 | missense variant | A/G | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 1.000 | 0.080 | 7 | 55191861 | missense variant | C/G | snv | 0.010 | 1.000 | 1 | 2006 | 2006 | |||||
|
2 | 1.000 | 0.080 | 7 | 55191845 | missense variant | G/A | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
2 | 0.925 | 0.120 | 7 | 55019290 | missense variant | G/C | snv | 0.010 | 1.000 | 1 | 2014 | 2014 |