The X-chromosome is often excluded from genome-wide association studies
because of analytical challenges. Some of the problems, such as the random,
skewed or no X-inactivation model uncertainty, have been investigated. Other
considerations have received little to no attention, such as the value in
considering non-additive and gene-sex interaction effects, and the inferential
consequence of choosing different baseline alleles (i.e.\ the reference vs.
the alternative allele). Here we propose a unified and flexible
regression-based association test for X-chromosomal variants. We provide
theoretical justifications for its robustness in the presence of various model
uncertainties, as well as for its improved power when compared with the
existing approaches under certain scenarios. For completeness, we also revisit
the autosomes and show that the proposed framework leads to a more robust
approach than the standard method. Finally, we provide supporting evidence by
revisiting several published association studies. Supplementary materials for
this article are available online.

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