{{Rsnum
|rsid=121909365
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=GHR
|position=42699830
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GHR
}}{{omim
|id=600946
|rsnum=121909365
|variant=0019
}}{{ClinVar
|rsid=121909365
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=42699932
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GHR:2690
|GENE_NAME=GHR
|GENE_ID=2690
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.42699932C>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000009183.1
|CLNDBN=Laron syndrome with undetectable serum GH-binding protein
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600946.0019
|Disease=Laron syndrome with undetectable serum GH-binding protein
}}