{{Rsnum
|rsid=1397048
|Gene=OR9G1
|Chromosome=11
|position=56466099
|Orientation=minus
|GMAF=0.466
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 14.2 | 49.6 | 36.3
| HCB | 3.6 | 38.0 | 58.4
| JPT | 1.8 | 38.9 | 59.3
| YRI | 60.5 | 33.3 | 6.1
| ASW | 29.8 | 54.4 | 15.8
| CHB | 3.6 | 38.0 | 58.4
| CHD | 0.9 | 37.6 | 61.5
| GIH | 9.9 | 32.7 | 57.4
| LWK | 56.9 | 38.5 | 4.6
| MEX | 10.5 | 33.3 | 56.1
| MKK | 36.4 | 53.2 | 10.4
| TSI | 16.7 | 46.1 | 37.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=17903294
|Trait=Hemostatic factors and hematological phenotypes
|Title=Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study
|RiskAllele=
|Pval=7.0000000000000005E-8
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PMID Auto
|PMID=20369022
|Title=Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1397048
|overall_frequency_n=64
|overall_frequency_d=126
|overall_frequency=0.507936
|n_genomes=38
|n_genomes_annotated=0
|n_haplomes=52
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}