{{Rsnum
|rsid=633185
|Gene=ARHGAP42
|Chromosome=11
|position=100722807
|Orientation=minus
|GMAF=0.348
|Gene_s=ARHGAP42
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 14.1 | 31.2 | 54.7
| HCB | 31.1 | 53.3 | 15.6
| JPT | 20.5 | 50.0 | 29.5
| YRI | 1.6 | 31.7 | 66.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 31.1 | 53.3 | 15.6
| 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
}}{{PMID Auto GWAS
|PMID=21909115
|Trait=None
|Title=Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|RiskAllele=G
|Pval=2E-15
|OR=0.3280
|ORtxt=[NR] mmHg decrease
|OA=1
}}
{{PMID Auto GWAS
|PMID=21909110
|Trait=None
|Title=Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
|RiskAllele=G
|Pval=7E-10
|OR=0.3250
|ORtxt=[0.22-0.43] mmHg decrease
|OA=1
}}