{{Rsnum
|rsid=17342647
|Gene=CYP3A43
|Chromosome=7
|position=99861633
|Orientation=plus
|GMAF=0.045
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CYP3A43
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 77.9 | 19.5 | 2.7
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 96.5 | 3.5 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 94.1 | 5.9 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 87.9 | 10.3 | 1.7
| MKK | 0.0 | 0.0 | 0.0
| TSI | 87.3 | 11.8 | 1.0
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs17342647
|Name_s=CYP3A43: 1150C>T; *1B; A349A
|Gene_s=CYP3A, CYP3A43
|Feature=Intron, Exon/Syn
|Evidence=PubMed ID:14695544
|Annotation=The CYP3A43*1B allele is characterized by the silent 1150C>T substitution exon 11.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Curated
|PharmGKB Accession ID=PA161845793
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17342647
|overall_frequency_n=904
|overall_frequency_d=10758
|overall_frequency=0.0840305
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}