{{Rsnum
|rsid=104894696
|Gene=HAMP
|Chromosome=19
|position=35284999
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=HAMP
}}{{omim
|id=606464
|rsnum=104894696
|variant=0004
}}{{ClinVar
|rsid=104894696
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=35775902
|CHROM=19
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=HAMP:57817
|GENE_NAME=HAMP
|GENE_ID=57817
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.35775902G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNACC=RCV000004507.1
|CLNDBN=Hemochromatosis, type 2a, modifier of
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606464.0004
|COMMON=0
|Disease=Hemochromatosis
}}