{{Rsnum
|rsid=387906549
|Chromosome=11
|position=61967589
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=FTH1
|Gene_s=FTH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=11
|CLNACC=RCV000017954.28
|CLNALLE=1
|CLNDBN=Hemochromatosis, type 5
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN181217:615517:247790
|CLNHGVS=NC_000011.9:g.61735061T>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134770.0001
|Disease=Hemochromatosis
|FwdALT=T
|FwdREF=A
|REF=T
|RSPOS=61735061
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=387906549
|GENEINFO=FTH1:2495
|GENE_ID=2495
|GENE_NAME=FTH1
}}