{{Rsnum
|rsid=2593813
|Gene=AHSG
|Chromosome=3
|position=186614782
|Orientation=minus
|GMAF=0.3393
|Gene_s=ACTBP7,AHSG
|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 | 13.3 | 40.7 | 46.0
| HCB | 8.8 | 40.1 | 51.1
| JPT | 3.5 | 43.4 | 53.1
| YRI | 17.7 | 48.3 | 34.0
| ASW | 25.0 | 41.1 | 33.9
| CHB | 8.8 | 40.1 | 51.1
| CHD | 10.1 | 47.7 | 42.2
| GIH | 3.0 | 29.7 | 67.3
| LWK | 6.4 | 40.9 | 52.7
| MEX | 17.2 | 51.7 | 31.0
| MKK | 4.5 | 37.2 | 58.3
| TSI | 8.8 | 39.2 | 52.0
| HapMapRevision=28
}}[[Category:is a snp]]

[http://cat.inist.fr/?aModele=afficheN&cpsidt=16815755] Homozygosity for the [[rs2593813]]:G-[[rs4917]]:Met-[[rs4918]]:Ser haplotype conferred an increased risk for leanness

{{omim
|desc=ALPHA-2-HS-GLYCOPROTEIN; AHSG
|id=138680
|rsnum=2593813
}}

{{PMID|15806395}} AHSG gene variant is associated with leanness among Swedish men.

{{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}}