{{Rsnum
|rsid=4918
|Gene=AHSG
|Chromosome=3
|position=186620593
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=C
|GMAF=0.3104
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=AHSG
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 46.2 | 36.9 | 16.9
| HCB | 33.3 | 55.6 | 11.1
| JPT | 52.3 | 45.5 | 2.3
| YRI | 45.2 | 45.2 | 9.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 33.3 | 55.6 | 11.1
| 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
}}[[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

{{ neighbor
| rsid = 4917
| distance = 669
}}

{{ neighbor
| rsid = 2518136
| distance = 555
}}

{{omim
|desc=ALPHA-2-HS-GLYCOPROTEIN; AHSG
|id=138680
|rsnum=4918
}}

{{PMID Auto
|PMID=20605840
|Title=Is fetuin-A a mortality risk factor in dialysis patients or a mere risk marker? A Mendelian randomization approach
}}

{{ClinVar
|rsid=4918
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=186338382
|CHROM=3
|GMAF=0.31
|dbSNPBuildID=52
|SSR=0
|SAO=1
|VP=0x05016800000017051f110101
|GENEINFO=AHSG:197
|GENE_NAME=AHSG
|GENE_ID=197
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.186338382G>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.3104; 0.6896
|CLNACC=RCV000017419.1
|CLNDBN=Leanness, susceptibility to
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=138680.0002
|COMMON=1
|Disease=Leanness
}}

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

{{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=17303000
|Title=Association and linkage analysis of COL1A1 and AHSG gene polymorphisms with femoral neck bone geometric parameters in both Caucasian and Chinese nuclear families.
}}

{{PMID Auto
|PMID=18805939
|Title=Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.
|OA=1
}}

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

{{GET Evidence
|gene=AHSG
|aa_change=Ser256Thr
|aa_change_short=S256T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4918
|overall_frequency_n=7086
|overall_frequency_d=10758
|overall_frequency=0.658673
|n_genomes=48
|n_genomes_annotated=0
|n_haplomes=69
|n_articles=0
|n_articles_annotated=0
|nblosum100=-2
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=23907641
|Title=Association of AHSG Gene Polymorphisms with Ischemic Stroke in a Han Chinese Population
}}

{{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}}