{{Rsnum
|rsid=121913153
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=INSR
|position=7267659
|Gene_s=INSR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=147670
|rsnum=121913153
|variant=0025
}}{{ClinVar
|rsid=121913153
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=7267670
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=INSR:3643
|GENE_NAME=INSR
|GENE_ID=3643
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.7267670C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=147670.0025
|CLNSIG=5
|CLNCUI=C0265344
|CLNDBN=Leprechaunism syndrome
|Disease=Leprechaunism syndrome
|CLNACC=RCV000015818.25
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0265344:246200:508:111307005
}}