{{Rsnum
|rsid=6013509
|Chromosome=20
|position=52701812
|Orientation=plus
|GMAF=0.3196
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 7.1 | 37.2 | 55.8
| HCB | 12.4 | 46.7 | 40.9
| JPT | 11.5 | 44.2 | 44.2
| YRI | 19.7 | 46.9 | 33.3
| ASW | 8.8 | 56.1 | 35.1
| CHB | 12.4 | 46.7 | 40.9
| CHD | 11.9 | 51.4 | 36.7
| GIH | 23.8 | 51.5 | 24.8
| LWK | 23.6 | 50.0 | 26.4
| MEX | 3.4 | 39.7 | 56.9
| MKK | 30.1 | 50.0 | 19.9
| TSI | 4.9 | 42.2 | 52.9
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19862010
|Trait=Hemoglobin
|Title=Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
|RiskAllele=A
|Pval=1E-10
|OR=0.06
|ORtxt=[0.05-0.08] g/dl decrease
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6013509
|overall_frequency_n=49
|overall_frequency_d=126
|overall_frequency=0.388889
|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 v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}