{{Rsnum
|rsid=121913136
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=INSR
|position=7170561
|Gene_s=INSR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=147670
|rsnum=121913136
|variant=0002
}}{{ClinVar
|rsid=121913136
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=7170572
|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.7170572T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=147670.0002
|CLNSIG=5
|CLNCUI=C0265344
|CLNDBN=Leprechaunism syndrome
|Disease=Leprechaunism syndrome
|CLNACC=RCV000015794.25
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0265344:246200:508:111307005
}}