{{Rsnum
|rsid = 28940586
|Gene = HFE2
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=C
|Chromosome=1
|position=146019594
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HFE2
}}{{omim
|desc=HEMOCHROMATOSIS, TYPE 2A
|id=608374
|rsnum=28940586
|variant=0005
}}

{{ClinVar
|rsid=28940586
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=146019594
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060480a05000002110100
|GENEINFO=HFE2:148738
|GENE_NAME=HFE2
|GENE_ID=148738
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.146019594A>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_213653.3:c.238T>C; 608374.0005
|CLNSIG=5
|CLNCUI=C1865614
|CLNDBN=Hemochromatosis type 2A
|Disease=Hemochromatosis type 2A
|CLNACC=RCV000002466.1
|Tags=RV;PM;NSM;REF;U5;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1170:C1865614:602390:ORPHA79230
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}