{{Rsnum
|rsid=9898
|Gene=HRG
|Chromosome=3
|position=186672838
|Orientation=plus
|GMAF=0.4633
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=HRG
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 43.2 | 46.8 | 9.9
| HCB | 26.5 | 41.9 | 31.6
| JPT | 26.8 | 50.9 | 22.3
| YRI | 12.2 | 42.2 | 45.6
| ASW | 24.6 | 49.1 | 26.3
| CHB | 26.5 | 41.9 | 31.6
| CHD | 22.0 | 49.5 | 28.4
| GIH | 40.6 | 41.6 | 17.8
| LWK | 19.3 | 42.2 | 38.5
| MEX | 38.6 | 47.4 | 14.0
| MKK | 6.4 | 45.5 | 48.1
| TSI | 33.7 | 50.5 | 15.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20303064
|Trait=Activated partial thromboplastin time
|Title=Common Variants of Large Effect in F12, KNG1, and HRG Are Associated with Activated Partial Thromboplastin Time
|RiskAllele=T
|Pval=1E-11
|OR=0.26
|ORtxt=[0.19-0.33] unit increase
|OA=1
}}

{{omim
|id=142640
|desc=HISTIDINE-RICH GLYCOPROTEIN; HRG
|rsnum=9898
}}

{{omim
|id=188050
|rsnum=9898
}}

{{PMID|21270443}} KNG1 Ile581Thr and susceptibility to venous thrombosis.

{{PMID Auto GWAS
|PMID=22703881
|Trait=None
|Title=Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease.
|RiskAllele=C
|Pval=1E-111
|OR=1.0000
|ORtxt=None
|OA=1
}}

{{GET Evidence
|gene=HRG
|aa_change=Pro204Ser
|aa_change_short=P204S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9898
|overall_frequency_n=4617
|overall_frequency_d=10758
|overall_frequency=0.429169
|n_genomes=34
|n_genomes_annotated=0
|n_haplomes=44
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=0
|webscore=N
}}

{{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}}