{{Rsnum
|rsid=9373124
|Chromosome=6
|position=135102071
|Orientation=plus
|GMAF=0.3356
|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 | 4.7 | 32.8 | 62.5
| HCB | 7.1 | 35.7 | 57.1
| JPT | 11.9 | 47.6 | 40.5
| YRI | 23.6 | 58.2 | 18.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 7.1 | 35.7 | 57.1
| 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
}}{{PMID Auto GWAS
|PMID=19862010
|Trait=Other erythrocyte phenotypes
|Title=Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
|RiskAllele=C
|Pval=7E-14
|OR=0
|ORtxt=[0.002-0.003] g/dl decrease
|OA=1
}}

{{PMID Auto GWAS
|PMID=21738478
|Trait=None
|Title=Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population.
|RiskAllele=T
|Pval=1E-10
|OR=0.0800
|ORtxt=[0.06-0.10] unit increase
|OA=1
}}
{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9373124
|overall_frequency_n=50
|overall_frequency_d=128
|overall_frequency=0.390625
|n_genomes=34
|n_genomes_annotated=0
|n_haplomes=43
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}