{{Rsnum
|rsid=2774279
|Gene=ARHGAP30
|Chromosome=1
|position=161047766
|Orientation=plus
|ReferenceAllele=G
|GMAF=0.2121
|Gene_s=ARHGAP30,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 | 33.6 | 48.7 | 17.7
| HCB | 78.1 | 19.0 | 2.9
| JPT | 81.4 | 16.8 | 1.8
| YRI | 71.4 | 27.2 | 1.4
| ASW | 64.9 | 35.1 | 0.0
| CHB | 78.1 | 19.0 | 2.9
| CHD | 68.8 | 28.4 | 2.8
| GIH | 44.6 | 45.5 | 9.9
| LWK | 70.0 | 29.1 | 0.9
| MEX | 58.6 | 36.2 | 5.2
| MKK | 81.4 | 17.9 | 0.6
| TSI | 40.2 | 49.0 | 10.8
| HapMapRevision=28
}}

{{PMID|18097648}}  The minor allele of [[rs2774279]] was less common among individuals with metabolic syndrome than among healthy controls [p = 0.0029; p = 0.0073]. The minor allele of rs2774279 was also associated with lower BMI, lower fasting glucose values and higher HDL-cholesterol concentrations in longitudinal analyses.

{{PMID Auto
|PMID=16699592
|Title=Risk alleles of USF1 gene predict cardiovascular disease of women in two prospective studies.
|OA=1
}}

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

{{PMID Auto
|PMID=18974842
|Title=Gender differences in genetic risk profiles for cardiovascular disease.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}