{{Rsnum
|rsid=387906399
|Chromosome=11
|position=2885179
|Orientation=minus
|geno1=(CT;CT)
|geno2=(CT;G)
|geno3=(G;G)
|Gene=CDKN1C
|Gene_s=CDKN1C
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=CC
|CHROM=11
|CLNACC=RCV000009289.2
|CLNALLE=1
|CLNDBN=Beckwith-Wiedemann syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1394:C0004903:130650:116:81780002
|CLNHGVS=NC_000011.9:g.2906409_2906410delAGinsC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600856.0003
|Disease=Beckwith-Wiedemann syndrome
|FwdALT=G
|FwdREF=CT
|REF=CAG
|RSPOS=2906408
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906399
|GENEINFO=CDKN1C:1028
|GENE_ID=1028
|GENE_NAME=CDKN1C
}}