Gene | Harmful genetic variants found in patients with TBE, that are not common in non-Finnish European populations | Harmful genetic variants associated with severe forms of TBE | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
SNP ID or SNV positiona | Exonic function | SIFT | Polyphen2 HDIV | Polyphen2 HVAR | N b | SNP ID | P-value | Exonic function | SIFT | Polyphen2 HDIV | |
MAP4 c | rs150907099 | nonsyn | D | D | D | 1 | rs11711953 | 0.001927 | nonsyn | D | D |
rs2230169 | 0.005399 | nonsyn | D | D | |||||||
WDFY4 | chr10:50,034,917 | nonsyn | D | D | D | 1 | rs41283283 | 0.003018 | nonsyn | T | D |
ACTRT2 | rs137950147 | nonsyn | T | D | P | 1 | rs3795263 | 0.009637 | nonsyn | D | D |
KLHL25 | rs779814173 | nonsyn | D | B | B | 1 | rs35582838 | 0.009274 | nonsyn | D | B |
MAP2K3 | rs141390631 | nonsyn | D | P | D | 1 | rs74575904 | 0.002442 | nonsyn | D | D |
MBD1 | rs183864846 | nonsyn | D | B | B | 1 | rs125555 | 0.009685 | nonsyn | D | P |
OR10J1 | rs35634161 | nonsyn | D | D | D | 2 | rs12048482 | 0.003306 | nonsyn | D | D |
rs12409540 | 0.005492 | stopgain | . | . | |||||||
OR2T34 | rs202166093 | nonsyn | D | D | D | 1 | rs199863869 | 0.001284 | nonsyn | D | B |