{{Rsnum
|rsid=1572983
|Gene=BAAT
|Chromosome=9
|position=101371346
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.3829
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=BAAT
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 11.5 | 45.1 | 43.4
| HCB | 14.0 | 38.2 | 47.8
| JPT | 10.6 | 58.4 | 31.0
| YRI | 25.2 | 59.9 | 15.0
| ASW | 17.5 | 54.4 | 28.1
| CHB | 14.0 | 38.2 | 47.8
| CHD | 19.3 | 47.7 | 33.0
| GIH | 28.7 | 42.6 | 28.7
| LWK | 28.4 | 50.5 | 21.1
| MEX | 20.7 | 41.4 | 37.9
| MKK | 22.7 | 49.4 | 27.9
| TSI | 9.8 | 39.2 | 51.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=1572983
|allele=T
|frequency=0.65
|uid=1103652142948
|type=homozygous_SNP
|hugo=BAAT
|ensembl gene=ENSG00000136881
|ensembl transcript=ENST00000259407
|sift=TOLERATED
|disease=Defects in BAAT are involved in familial hypercholanemia (FHCA) (MIM:607748). FHCA is a disorder characterized by elevated serum bile acid concentrations, itching, and fat malabsorption.
}}

{{ neighbor
| rsid = 28937579
| distance = 167
}}

{{PMID|17495420}} Genetic polymorphism of bile acid CoA: amino acid N-acyltransferase in Japanese individuals.

{{GET Evidence
|gene=BAAT
|aa_change=Arg20Gln
|aa_change_short=R20Q
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1572983
|overall_frequency_n=6742
|overall_frequency_d=10758
|overall_frequency=0.626696
|n_genomes=48
|n_genomes_annotated=0
|n_haplomes=74
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.136
|genetests_testable=Y
|nblosum100=0
|autoscore=2
|n_web_uneval=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}