{{Rsnum
|rsid=61730328
|Gene=ZFP57
|Chromosome=6
|position=29673328
|Orientation=plus
|GMAF=0.005051
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=ZFP57
}}{{omim
|id=612192
|rsnum=61730328
|variant=0001
}}{{ClinVar
|rsid=61730328
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=29641105
|CHROM=6
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050268000000040516110100
|GENEINFO=ZFP57:346171
|GENE_NAME=ZFP57
|GENE_ID=346171
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000006.11:g.29641105G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=612192.0001
|CLNSIG=5
|CLNCUI=C1832386; C1832386
|CLNDBN=Transient neonatal diabetes mellitus 1
|Disease=Transient neonatal diabetes mellitus 1
|CLNACC=RCV000000751.1
|Tags=PM;PMC;S3D;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9949; 0.005051; .
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1534:C1832386:601410
|COMMON=1
}}{{PMID|18197189}} Clinical characterisation of the multiple maternal hypomethylation syndrome in siblings.

{{PMID|18622393}} Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57.