Hi Open Targets team,
with the new genetics-portal focus on retaining credible set variants only, some discrepancies in variant coverage to the former open targets genetics portal would be expected. Has this been quantified in any way? One example we found is following variant being present in open target genetics but not the new open targets platform:
9_89042048_T_C | Open Targets Genetics
Or could there be other reasons for this variant not being present in new open targets platform anymore?
Many thanks, Stefanie