{{Rsnum
|rsid = 34838342
|Gene = GHR
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=5
|position=42565884
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GHR
}}{{Venter SNP
|rsid=34838342
|allele=C
|frequency=
|uid=1103654086484
|type=heterozygous_SNP
|hugo=GHR
|ensembl gene=ENSG00000112964
|ensembl transcript=ENST00000356276
|sift=TOLERATED
|disease=Defects in GHR are a cause of idiopathic short stature (ISS) (MIM:600946). ISS is defined by a subnormal rate of growth.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}