{{Rsnum
|rsid=74315326
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HFE2
|position=146018516
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HFE2
}}{{omim
|id=608374
|rsnum=74315326
|variant=0004
}}{{ClinVar
|rsid=74315326
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=146018516
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=HFE2:148738
|GENE_NAME=HFE2
|GENE_ID=148738
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.146018516A>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_213653.3:c.842T>C; 608374.0004
|CLNSIG=5
|CLNCUI=C1865614
|CLNDBN=Hemochromatosis type 2A
|Disease=Hemochromatosis type 2A
|CLNACC=RCV000002465.1
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1170:C1865614:602390:ORPHA79230
}}