{{Rsnum
|rsid=104894517
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HP
|position=72060409
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HP,TXNL4B
}}{{omim
|id=140100
|rsnum=104894517
|variant=0005
}}{{ClinVar
|rsid=104894517
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=72094308
|CHROM=16
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050260000000000002110100
|GENEINFO=HP:3240
|GENE_NAME=HP
|GENE_ID=3240
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.72094308T>C
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=140100.0005
|CLNSIG=255
|CLNCUI=CN071106; CN071106
|CLNDBN=Anhaptoglobinemia
|Disease=Anhaptoglobinemia
|CLNACC=RCV000017249.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3279786:614081
}}