same in each study. In the Mendelian randomization context, we can test whether causal estimates from different genetic variants are compatible. Considerable heterogeneity would be evidence that the genetic variants are estimating different quantities, and would cast doubt on the IV assumptions being valid for all the variants. In IV analysis more generally, a heterogeneity test is equivalent to an over-identification test, often performed with individual-level data as part of a TSLS analysis.48