It seems the REST API still returns wrong chr positions for the genomic contexts in the variants responses, i.e. the positions are those of the variants and not of the associated genes (as meant to be).
Any plans to fix this? I think this is a really old bug...
It seems the REST API still returns wrong chr positions for the genomic contexts in the variants responses, i.e. the positions are those of the variants and not of the associated genes (as meant to be).
Any plans to fix this? I think this is a really old bug...