{{Rsnum
|rsid=28914832
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC6A4
|position=30211356
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC6A4
}}{{omim
|id=182138
|rsnum=28914832
|variant=0002
}}

{{ClinVar
|rsid=28914832
|Reversed=1
|FwdREF=A
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=28538374
|CHROM=17
|dbSNPBuildID=125
|SSR=0
|SAO=1
|VP=0x050268000000040102110100
|GENEINFO=SLC6A4:6532
|GENE_NAME=SLC6A4
|GENE_ID=6532
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.28538374T>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;VLD;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000013798.1
|CLNDBN=Obsessive-compulsive disorder, susceptibility to
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=182138.0002
|Disease=Obsessive-compulsive disorder
}}

{{PMID|15995945|OA=1
}} Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

{{PMID|18957375|OA=1
}} Enhanced activity of human serotonin transporter variants associated with autism.

{{PMID|19032574|OA=1
}} Characterization of a functional polymorphism in the 3' UTR of SLC6A4 and its association with drinking intensity.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}