{{Rsnum
|rsid=121918229
|Chromosome=6
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=CUL7
|position=43038891
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CUL7
}}{{omim
|id=609577
|rsnum=121918229
|variant=0002
}}{{ClinVar
|rsid=121918229
|Reversed=1
|FwdREF=A
|FwdALT=C
|REF=T
|ALT=G
|RSPOS=43006629
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CUL7:9820
|GENE_NAME=CUL7
|GENE_ID=9820
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.43006629T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609577.0002
|CLNSIG=5
|CLNCUI=C1848862
|CLNDBN=Three M syndrome 1
|Disease=Three M syndrome 1
|CLNACC=RCV000001681.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1481:C1848862:273750:2616
}}