{{Rsnum
|rsid=16926246
|Gene=HK1
|Chromosome=10
|position=71093392
|Orientation=plus
|GMAF=0.09963
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 78.1 | 21.9 | 0.0
| HCB | 95.3 | 4.7 | 0.0
| JPT | 97.6 | 2.4 | 0.0
| YRI | 66.7 | 30.2 | 3.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 95.3 | 4.7 | 0.0
| 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=Hematocrit
|Title=Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
|RiskAllele=T
|Pval=1E-13
|OR=0.33
|ORtxt=[0.24-0.42] % increase
|OA=1
}}
{{PMID Auto
|PMID=20858683
|Title=Common variants at ten genomic loci influence hemoglobin A1C levels via glycemic and non-glycemic pathways
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs16926246
|overall_frequency_n=14
|overall_frequency_d=128
|overall_frequency=0.109375
|n_genomes=15
|n_genomes_annotated=0
|n_haplomes=15
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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