{{Rsnum
|rsid=3760091
|Gene=SULT1A1
|Chromosome=16
|position=28609479
|Orientation=plus
|GMAF=0.3838
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=SULT1A1
}}{{PharmGKB
|RSID=rs3760091
|Name_s=SULT1A1: -624G>C
|Gene_s=SULT1A1
|Feature=Intron
|Evidence=PubMed ID:15970794
|Annotation=This promoter region SNP is tightly linked to the *2 variant and may be responsible for functional effects that have been attributed to *2.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Curated
|PharmGKB Accession ID=PA161845803
}}

{{PharmGKB
|RSID=rs3760091
|Name_s=SULT1A1:-624G>C
|Gene_s=SULT1A1
|Feature=Intron
|Evidence=Web Resource:http://www.pharmgkb.org/search/annotatedGene/sult1a1/variant.jsp
|Annotation=Associated with increased activity in vitro.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=In-Depth
|PharmGKB Accession ID=PA161145156
}}{{PMID Auto
|PMID=19287157
|Title=Sulfotransferase gene copy number variation: pharmacogenetics and function.
|OA=1
}}{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3760091
|overall_frequency_n=50
|overall_frequency_d=128
|overall_frequency=0.390625
|n_genomes=38
|n_genomes_annotated=0
|n_haplomes=44
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}