Dear all:
First of all, thanks for the great package!
I just have a naive question since I am pretty new to fine-mapping process. For my research objective, I plan to fine-map 5 particular variants with CHR, BP, A1, A2, EAF, BETA, and SE. I know that PolyFun is advanced in handling in fine-mapping GWAS summary statitistics. I just wonder in my case (fine map only 5 SNPs), is the PolyFun tool and subsequent SuSiE going to produce reliable results? Or if it is mandatory to have the summary statistics for the analysis pipeline?

I would really appreciate your insights.
Best,
Jackson