{{Rsnum
|rsid=121908278
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=INS
|position=2160956
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=INS,INS-IGF2
}}{{omim
|id=176730
|rsnum=121908278
|variant=0014
}}{{ClinVar
|rsid=121908278
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=2182186
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050168000000000002110100
|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.2182186G>A
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=176730.0014; VAR_063721
|CLNSIG=5
|CLNCUI=C3150617
|CLNDBN=Maturity-onset diabetes of the young, type 10
|Disease=Maturity-onset diabetes of the young
|CLNACC=RCV000014322.24
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3150617:613370:552
}}{{PMID|18162506}} Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.