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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
5 | 0.851 | 0.160 | X | 114903581 | intron variant | C/G | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||
|
34 | 0.716 | 0.600 | 6 | 157181056 | stop gained | C/A;T | snv | 0.700 | 1.000 | 2 | 2012 | 2015 | |||||
|
6 | 0.851 | 0.320 | 10 | 87933175 | stop gained | T/G | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.040 | 2 | 161417827 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.040 | 2 | 161418249 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
4 | 0.882 | 0.200 | 2 | 25247710 | stop gained | T/A;G | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.040 | 3 | 1295712 | stop gained | C/A | snv | 0.700 | 0 | ||||||||
|
5 | 0.882 | 0.160 | 18 | 33739086 | stop gained | C/A | snv | 0.700 | 0 | ||||||||
|
6 | 0.882 | 0.320 | 16 | 89280070 | stop gained | C/A | snv | 0.700 | 0 | ||||||||
|
9 | 0.851 | 0.200 | 11 | 687941 | missense variant | C/T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
6 | 0.882 | 0.160 | 7 | 39686740 | missense variant | G/A | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||
|
4 | 0.882 | 0.280 | 11 | 1443490 | missense variant | G/A | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
14 | 0.851 | 0.240 | 11 | 686925 | missense variant | C/G | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
249 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 0.010 | 1.000 | 1 | 2020 | 2020 | |||
|
46 | 0.695 | 0.400 | 10 | 129957324 | missense variant | C/A;G;T | snv | 0.700 | 0 | ||||||||
|
4 | 0.882 | 0.120 | 10 | 87894076 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
5 | 0.882 | 0.120 | 10 | 87864504 | missense variant | A/C | snv | 0.700 | 0 | ||||||||
|
8 | 0.807 | 0.160 | 10 | 87933128 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
9 | 0.790 | 0.240 | 10 | 87933160 | missense variant | T/C;G | snv | 0.700 | 0 | ||||||||
|
6 | 0.827 | 0.160 | 10 | 87864509 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
6 | 0.882 | 0.200 | 10 | 87933229 | missense variant | A/G | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
14 | 0.776 | 0.280 | 10 | 87952143 | missense variant | G/A;C;T | snv | 8.0E-06 | 0.700 | 0 | |||||||
|
2 | 1.000 | 0.040 | 2 | 161417083 | missense variant | A/T | snv | 0.700 | 0 | ||||||||
|
3 | 0.925 | 0.040 | 2 | 161417794 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
4 | 1.000 | 0.040 | 12 | 13569964 | missense variant | C/A | snv | 0.700 | 0 |