{{Rsnum
|rsid=121918101
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=INS
|position=2160872
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=INS,INS-IGF2
}}{{omim
|id=176730
|rsnum=121918101
|variant=0003
}}{{ClinVar
|rsid=121918101
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=2182102
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=INS:3630; INS-IGF2:723961
|GENE_NAME=INS; INS-IGF2
|GENE_ID=3630; 723961
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.2182102G>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000014308.24; RCV000014309.24
|CLNDBN=Hyperproinsulinemia, familial; Proinsulin providence
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=176730.0003
|Disease=Hyperproinsulinemia; Proinsulin providence
}}