{{Rsnum
|rsid=74315323
|Chromosome=1
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=HFE2
|position=146018399
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HFE2
}}{{omim
|id=608374
|rsnum=74315323
|variant=0001
}}{{ClinVar
|rsid=74315323
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=146018399
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050060000a05040402110100
|GENEINFO=HFE2:148738
|GENE_NAME=HFE2
|GENE_ID=148738
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.146018399C>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_213653.3:c.959G>T; 608374.0001
|CLNSIG=5
|CLNCUI=C1865614; C0392514
|CLNDBN=Hemochromatosis type 2A; Hereditary hemochromatosis
|Disease=Hemochromatosis type 2A; Hereditary hemochromatosis
|CLNACC=RCV000002461.1; RCV000002462.1
|Tags=RV;PM;NSM;REF;ASP;VLD;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1170:C1865614:602390:ORPHA79230; NBK1440:C0392514:235200:35400008
}}