{{Rsnum
|rsid=2518136
|Gene=AHSG
|Chromosome=3
|position=186620038
|Orientation=plus
|GMAF=0.4927
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=AHSG
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 29.5 | 44.6 | 25.9
| HCB | 40.7 | 46.7 | 12.6
| JPT | 36.3 | 44.2 | 19.5
| YRI | 8.8 | 43.5 | 47.6
| ASW | 12.5 | 32.1 | 55.4
| CHB | 40.7 | 46.7 | 12.6
| CHD | 33.9 | 50.5 | 15.6
| GIH | 34.7 | 50.5 | 14.9
| LWK | 13.8 | 44.0 | 42.2
| MEX | 13.8 | 62.1 | 24.1
| MKK | 20.0 | 52.9 | 27.1
| TSI | 28.7 | 50.5 | 20.8
| HapMapRevision=28
}}

{{PMID|18316360}} Associated with [[type-2 diabetes]] in a study of Danish (but apparently not Swedish or French) Caucasians

{{ neighbor
| rsid = 4917
| distance = 114
}}
{{ neighbor
| rsid = 4918
| distance = 555
}}

{{PMID Auto
|PMID=22024217
|Title=Are AHSG polymorphisms directly associated with coronary atherosclerosis?
}}

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