Hi @sosaar, and welcome to the Open Targets Community!
I’m not sure I understand your question.
In the post you are referring to, Andrew used FINNGEN_R5_E4_DM2 as an example of new data in Open Targets Genetics, but you could apply the same code to a different study (not necessarily one from FinnGen), by replacing the study and variant IDs with the ones you are interested in — see an example in the API Playground.
Let me know if this answers your question!
Helena