{{Rsnum
|rsid=137852766
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CDKN1C
|position=2885351
|Gene_s=CDKN1C
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600856
|variant=0001
|rsnum=137852766
}}{{ClinVar
|rsid=137852766
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=2906581
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CDKN1C:1028
|GENE_NAME=CDKN1C
|GENE_ID=1028
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.2906581G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600856.0001
|CLNSIG=5
|CLNCUI=C0004903
|CLNDBN=Beckwith-Wiedemann syndrome
|Disease=Beckwith-Wiedemann syndrome
|CLNACC=RCV000009287.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1394:C0004903:130650:116:81780002
}}