{{Rsnum
|rsid=1071592
|Gene=AHSG
|Chromosome=3
|position=186620636
|Orientation=plus
|ReferenceAllele=A
|GMAF=0.2121
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=AHSG
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 10.7 | 35.7 | 53.6
| HCB | 2.9 | 31.4 | 65.7
| JPT | 1.8 | 25.7 | 72.6
| YRI | 0.0 | 29.3 | 70.7
| ASW | 3.5 | 33.3 | 63.2
| CHB | 2.9 | 31.4 | 65.7
| CHD | 5.5 | 32.1 | 62.4
| GIH | 0.0 | 16.8 | 83.2
| LWK | 0.9 | 16.4 | 82.7
| MEX | 5.2 | 56.9 | 37.9
| MKK | 1.9 | 17.9 | 80.1
| TSI | 2.0 | 30.4 | 67.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=19358088
|Title=AHSG Gene Variation is not Associated with Regional Body Fat Distribution - A Magnetic Resonance Study.
}}

{{PMID Auto
|PMID=16046317
|Title=A synonymous coding polymorphism in the alpha2-Heremans-schmid glycoprotein gene is associated with type 2 diabetes in French Caucasians.
}}

{{PMID Auto
|PMID=19098027
|Title=SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms.
|OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}