{{Rsnum
|rsid=121909367
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GHR
|position=42699896
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GHR
}}{{omim
|id=600946
|rsnum=121909367
|variant=0022
}}{{ClinVar
|rsid=121909367
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=42699998
|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.42699998T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600946.0022
|CLNSIG=5
|CLNCUI=C0271568
|CLNDBN=Laron-type isolated somatotropin defect
|Disease=Laron-type isolated somatotropin defect
|CLNACC=RCV000009186.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0271568:262500:633:38196001
}}