{{Rsnum
|rsid=121908088
|Gene=TPO
|Chromosome=2
|position=1494011
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=TPO
}}{{omim
|id=606765
|rsnum=121908088
|variant=0014
}}{{ClinVar
|rsid=121908088
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=1497783
|CHROM=2
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000016110100
|GENEINFO=TPO:7173
|GENE_NAME=TPO
|GENE_ID=7173
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.1497783C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606765.0014
|CLNSIG=5
|CLNCUI=C1291299
|CLNDBN=Deficiency of iodide peroxidase
|Disease=Deficiency of iodide peroxidase
|CLNACC=RCV000004268.1
|Tags=PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1291299:274500:95716:124204003
|COMMON=0
}}