{{Rsnum
|rsid=52836744
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=INSR
|position=7267825
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=INSR
}}{{omim
|id=147670
|rsnum=52836744
|variant=0020
}}{{ClinVar
|rsid=52836744
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=7267836
|CHROM=19
|dbSNPBuildID=128
|SSR=0
|SAO=1
|VP=0x050260000000000502110100
|GENEINFO=INSR:3643
|GENE_NAME=INSR
|GENE_ID=3643
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.7267836C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=147670.0020
|CLNSIG=5
|CLNCUI=C0265344
|CLNDBN=Leprechaunism syndrome
|Disease=Leprechaunism syndrome
|CLNACC=RCV000015814.25
|Tags=RV;PM;S3D;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0265344:246200:508:111307005
}}