{{Rsnum
|rsid=3737787
|Gene=USF1
|Chromosome=1
|position=161039733
|Orientation=minus
|GMAF=0.2158
|Gene_s=TSTD1,USF1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 53.1 | 39.8 | 7.1
| HCB | 58.1 | 36.0 | 5.9
| JPT | 61.1 | 36.3 | 2.7
| YRI | 94.6 | 5.4 | 0.0
| ASW | 78.9 | 21.1 | 0.0
| CHB | 58.1 | 36.0 | 5.9
| CHD | 67.9 | 30.3 | 1.8
| GIH | 73.3 | 26.7 | 0.0
| LWK | 88.1 | 11.9 | 0.0
| MEX | 50.9 | 43.9 | 5.3
| MKK | 77.6 | 20.5 | 1.9
| TSI | 54.9 | 36.3 | 8.8
| HapMapRevision=28
}}
{{omim
|desc=HYPERLIPIDEMIA, FAMILIAL COMBINED, SUSCEPTIBILITY TO
|id=191523
|rsnum=3737787
|variant=0001
}}

{{PMID|17673701}} contributes to high serum lipid levels in Dutch familial combined hyperlipidemia families and U.S. whites with coronary artery disease

{{PMID Auto
|PMID=19750004
|Title=A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia
|OA=1
}}

{{PMID|15657872|OA=1
}} Association testing in a linked region using large pedigrees.

{{PMID|15959806}} Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides.

{{PMID|15976322}} Familial combined hyperlipidemia in Mexicans: association with upstream transcription factor 1 and linkage on chromosome 16q24.1.

{{PMID|16132950}} The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population.

{{PMID|16186412}} Common polymorphisms in the USF1 gene are not associated with type 2 diabetes in French Caucasians.

{{PMID|16936202}} Variation within the gene encoding the upstream stimulatory factor 1 does not influence susceptibility to type 2 diabetes in samples from populations with replicated evidence of linkage to chromosome 1q.

{{PMID|18067551}} Association of F11 receptor gene polymorphisms with central obesity and blood pressure.

{{PMID|18276913|OA=1
}} Association analysis of allelic variants of USF1 in coronary atherosclerosis.

{{PMID|18303204|OA=1
}} Body mass index is associated with USF1 haplotype in Korean premenopausal women.

{{PMID|18445538}} Upstream transcription factor 1 (USF1) in risk of type 2 diabetes: association study in 2000 Dutch Caucasians.

{{PMID|18577828}} Allelic variants of upstream transcription factor 1 associate with carotid artery intima-media thickness: the Cardiovascular Risk in Young Finns study.

{{PMID|18593823}} Genetic variants in the USF1 gene are associated with low-density lipoprotein cholesterol levels and incident type 2 diabetes mellitus in women: results from the MONICA/KORA Augsburg case-cohort study, 1984-2002.

{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000013088.1
|CLNALLE=1
|CLNDBN=Hyperlipidemia, familial combined, susceptibility to
|CLNHGVS=NC_000001.11:g.161039733G>A
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_001113205.1:c.-844C>T; NM_007122.4:c.*187C>T; 191523.0001
|Disease=Hyperlipidemia
|FwdALT=T
|FwdREF=C
|GENEINFO=TSTD1:100131187; USF1:7391
|GENE_ID=100131187; 7391
|GENE_NAME=TSTD1; USF1
|REF=G
|RSPOS=161039733
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;U3;R5;ASP;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;OM
|VC=SNV
|VP=0x05016882000515051f010100
|WGT=1
|dbSNPBuildID=107
|rsid=3737787
}}
{{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}}