{{Rsnum
|rsid=104894695
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HAMP
|position=35284953
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HAMP
}}{{omim
|id=606464
|rsnum=104894695
|variant=0002
}}{{ClinVar
|rsid=104894695
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=35775856
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=HAMP:57817
|GENE_NAME=HAMP
|GENE_ID=57817
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.35775856C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606464.0002
|CLNSIG=5
|CLNCUI=C1865616
|CLNDBN=Hemochromatosis type 2B
|Disease=Hemochromatosis type 2B
|CLNACC=RCV000004505.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1170:C1865616:613313:79230
}}