{{Rsnum
|rsid=4986908
|Gene=CYP3A4
|Chromosome=7
|position=99769769
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.002296
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CYP3A4
}}[[rs4986908]] is a SNP in the [[CYP3A4]] gene.

The [[rs4986908]](A) allele defines the CYP3A4*_14313G>A(E174H) variant.

{{PharmGKB
|RSID=rs4986908
|Name_s=CYP3A4:D174H; CYP3A4:624 G>C; CYP3A4*10
|Gene_s=CYP3A, CYP3A4
|Feature=
|Evidence=Web Resource:http://www.pharmgkb.org/search/annotatedGene/cyp3a4/haplotype.jsp#ImportantHaplotypeInformationforCYP3A4-28
|Annotation=Defining variant for CYP3A4*10.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=In-Depth
|PharmGKB Accession ID=PA161145177
}}

{{ population diversity
| geno1 = (A;G)
| geno2 = (G;G)
| geno3 = 
| CEU | 0 | 0 | 0
| CHB | 2.3 | 97.7 | 0
| JPT | 0 | 0 | 0
| YRI | 0 | 0 | 0
}}

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