{{Rsnum
|rsid=198846
|Gene=HIST1H1T
|Chromosome=6
|position=26107235
|Orientation=plus
|GMAF=0.124
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=HIST1H1T
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 29.2 | 69.9
| HCB | 0.0 | 6.6 | 93.4
| JPT | 0.0 | 7.1 | 92.9
| YRI | 2.0 | 35.4 | 62.6
| ASW | 3.5 | 15.8 | 80.7
| CHB | 0.0 | 6.6 | 93.4
| CHD | 0.0 | 5.5 | 94.5
| GIH | 0.0 | 16.8 | 83.2
| LWK | 2.7 | 22.7 | 74.5
| MEX | 0.0 | 27.6 | 72.4
| MKK | 1.9 | 21.8 | 76.3
| TSI | 3.9 | 26.5 | 69.6
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19820698
|Trait=Hemoglobin levels
|Title=Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels
|RiskAllele=A
|Pval=1E-8
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PMID Auto GWAS
|PMID=21909110
|Trait=None
|Title=Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
|RiskAllele=G
|Pval=2E-12
|OR=0.4780
|ORtxt=[0.35-0.61] mmHg decrease
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs198846
|overall_frequency_n=114
|overall_frequency_d=128
|overall_frequency=0.890625
|n_genomes=55
|n_genomes_annotated=0
|n_haplomes=98
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}