Relativistic calculations of (29)Si NMR shielding constants (chemical shifts) in the series of halosilanes SiX(n)H(4-n) (X = F, Cl, Br and I) are performed within a full four-component relativistic Dirac's scheme using relativistic Dyall's basis sets. Three different theoretical levels are tested in the computation of (29)Si NMR chemical shifts in comparison with experiment: namely, four-component relativistic GIAO-DFT, four-component relativistic GIAO-RPA, and a hybrid scheme of a nonrelativistic GIAO-MP2 with taking into account relativistic corrections using the four-component relativistic GIAO-RPA. The DFT results give larger relativistic effects as compared to the RPA data which might be rationalized in terms of the manifestation of correlation effects taken into account at the DFT level and not accounted for at the uncorrelated RPA level. Taking into account solvent effects slightly improves agreement with experiment, however, being not a matter of principle. Generally, relativistic pure nonempirical wave function methods perform much better as compared to relativistic DFT methods when benchmarked to experiment.