{{Rsnum
|rsid = 28933985
|Gene = INS
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=11
|position=2159919
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=INS,INS-IGF2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.9 | 99.1
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=HYPERPROINSULINEMIA, FAMILIAL
|id=176730
|rsnum=28933985
|variant=0004
}}

{{omim
|id=176730
|rsnum=28933985
|variant=0006
}}

{{omim
|id=176730
|rsnum=28933985
|variant=0007
}}

{{ClinVar
|rsid=28933985
|Reversed=1
|FwdREF=G
|FwdALT=A,C,T
|REF=C
|ALT=A,G,T
|RSPOS=2181149
|CHROM=11
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000000402110104
|GENEINFO=INS:3630; INS-IGF2:723961
|GENE_NAME=INS; INS-IGF2
|GENE_ID=3630; 723961
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000011.9:g.2181149C>A; NC_000011.9:g.2181149C>G; NC_000011.9:g.2181149C>T
|CLNORIGIN=1
|CLNSRCID=
176730.0006; 176730.0007; 176730.0004
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000014313.23; RCV000014314.25; RCV000014315.23; RCV000014310.23
|Tags=RV;PM;S3D;HD;OTHERKG;LSD;OM;NOV
|CLNDBN=Hyperproinsulinemia, familial; Proinsulin kyoto
|CLNSRC=OMIM Allelic Variant
|Disease=Hyperproinsulinemia; Proinsulin kyoto
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}