{{Rsnum
|rsid=6413484
|Gene=GHR
|Chromosome=5
|position=42699868
|Orientation=plus
|GMAF=0.005969
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=GHR
}}{{omim
|id=600946
|rsnum=6413484
|variant=0020
}}

{{ population diversity
| geno1 = (G;G)
| geno2 = 
| geno3 = 
| CEU | 100.0 | 0 | 0
| CHB | 100.0 | 0 | 0
| JPT | 100.0 | 0 | 0
| YRI | 100.0 | 0 | 0
}}

{{ClinVar
|rsid=6413484
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=42699970
|CHROM=5
|GMAF=0.0064
|dbSNPBuildID=116
|SSR=0
|SAO=1
|VP=0x050360000000040517110100
|GENEINFO=GHR:2690
|GENE_NAME=GHR
|GENE_ID=2690
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.42699970G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600946.0020
|CLNSIG=5
|CLNCUI=C1858656
|CLNDBN=Short stature, idiopathic, autosomal
|Disease=Short stature
|CLNACC=RCV000009184.1
|Tags=PM;S3D;SLO;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.994; 0.005969; .
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1858656:604271:314811
|COMMON=1
}}

{{GET Evidence
|gene=GHR
|aa_change=Val162Ile
|aa_change_short=V162I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6413484
|overall_frequency_n=35
|overall_frequency_d=10758
|overall_frequency=0.00325339
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=-4
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}