{{Rsnum
|rsid=137853233
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HP
|position=72057415
|Gene_s=HP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=140100
|variant=0001
|rsnum=137853233
}}{{ClinVar
|rsid=137853233
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=72091314
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=HP:3240
|GENE_NAME=HP
|GENE_ID=3240
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.72091314A>G
|CLNORIGIN=1
|CLNSIG=2
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000017244.1
|CLNDBN=HAPTOGLOBIN, ALPHA-1, FAST-SLOW POLYMORPHISM
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=140100.0001
|Disease=HAPTOGLOBIN
}}