{{Rsnum
|rsid=1042157
|Gene=SULT1A1
|Chromosome=16
|position=28605736
|Orientation=minus
|GMAF=0.2952
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SULT1A1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 65.9 | 27.3 | 6.8
| JPT | 59.1 | 38.6 | 2.3
| YRI | 75.0 | 25.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 65.9 | 27.3 | 6.8
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs1042157
|Name_s=SULT1A1:85C/T
|Gene_s=SULT1A1, SULT1A2
|Feature=
|Evidence=PubMed ID:18318428
|Annotation=In one case-control study of SF Bay Area Caucasians, a haplotype containing the variant alleles of rs9282861,rs6839 and rs1042157 was associated with increased risk of endometrial cancer.
|Drugs=
|Drug Classes=
|Diseases=Endometrial Neoplasms
|Curation Level=Curated
|PharmGKB Accession ID=PA161845806
}}

{{PMID Auto
|PMID=20881232
|Title=Functional genetic variants in the 3'-untranslated region of sulfotransferase isoform 1A1 (SULT1A1) and their effect on enzymatic activity.
|OA=1
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1042157
|overall_frequency_n=31
|overall_frequency_d=128
|overall_frequency=0.242188
|n_genomes=27
|n_genomes_annotated=0
|n_haplomes=28
|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 | HumanOmni1Quad}}