Those are good general purpose filters. Depending on how variants were called, you might have the option to filter on other fields depending on your needs (say, if the VCF was generated by calling haplotypes in the GATK or something). Hardy-Weinberg Equilibrium filtering is also helpful in identifying and removing potentially paralogous sites resulting from misplaced reads, but it's usually an additional analysis done after you have a multisample VCF.