{{Rsnum
|rsid=193929361
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ABCC8
|position=17474919
|Gene_s=ABCC8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=193929360
}}{{ClinVar
|rsid=193929361
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=17496466
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=0
|VP=050168000a11000002110100
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.17496466A>C
|CLNSRC=OMIM Allelic Variant; GeneReviews
|CLNORIGIN=0
|CLNSRCID=600509.0026; NBK1447
|CLNSIG=5
|CLNCUI=C1833104; C1833104
|CLNDBN=Permanent neonatal diabetes mellitus
|Disease=Permanent neonatal diabetes mellitus
|CLNACC=SCV000029899.1; SCV000040643.1
|Tags=RV;PM;PMC;SLO;NSM;REF;OTH;OTHERKG;LSD;OM
}}{{PMID Auto
|PMID=17668386
|Title=Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects.
|OA=1
}}