{{Rsnum
|rsid=1800730
|Gene=HFE
|Chromosome=6
|position=26090957
|Orientation=plus
|GMAF=0.007346
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=HFE
}}a mild form of [[hemochromatosis]] {{PMID|10194428}}; in SNPedia, see also [[i3002468]]

{{omim
|id=613609
|rsnum=1800730
|variant=0003
}}

{{ClinVar
|rsid=1800730
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=26091185
|CHROM=6
|GMAF=0.0073
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050368000000040416110100
|GENEINFO=HFE:3077
|GENE_NAME=HFE
|GENE_ID=3077
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.26091185A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=613609.0003
|CLNSIG=5
|CLNCUI=C0392514
|CLNDBN=Hereditary hemochromatosis
|Disease=Hereditary hemochromatosis
|CLNACC=RCV000000028.2
|Tags=PM;PMC;S3D;SLO;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9927; 0.007346
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1440:C0392514:235200:35400008
|COMMON=1
}}

{{PMID Auto
|PMID=23792061
|Title=Meta-analyses of HFE variants in coronary heart disease
}}

{{on chip | HumanOmni1Quad}}