Unfortunately there hasn't been much research into these genes at all, aside from case studies involving the extreme cases. All of the ones listed are missense mutations, though the ACAT2 mutation is common for all variations - probably because the mutation results in one amino acid being replaced by an almost identical amino acid, resulting in little or no change in functionality of the gene.
There's no research associated with Yasko ACAT1 SNP, hence no reason to believe it has an impact, thus it's not on this list.
ACAT1
rsID.........NAME....RISK...ETC
rs120074142..M1K.....AA...i5002143
rs120074145..N93S....G....i5002140
rs120074146..I312T...C....i5002139
rs120074147..A333P...C....i5002138
rs120074143..G379V...T....i5002142
ACAT2
rsID.........NAME....RISK...ETC
rs25683......K211R...??
There's no research associated with Yasko ACAT1 SNP, hence no reason to believe it has an impact, thus it's not on this list.
ACAT1
rsID.........NAME....RISK...ETC
rs120074142..M1K.....AA...i5002143
rs120074145..N93S....G....i5002140
rs120074146..I312T...C....i5002139
rs120074147..A333P...C....i5002138
rs120074143..G379V...T....i5002142
ACAT2
rsID.........NAME....RISK...ETC
rs25683......K211R...??