{{Rsnum
|rsid=121918228
|Gene=CUL7
|Chromosome=6
|position=43038949
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CUL7
}}{{omim
|id=609577
|rsnum=121918228
|variant=0001
}}{{ClinVar
|rsid=121918228
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=43006687
|CHROM=6
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|GENEINFO=CUL7:9820
|GENE_NAME=CUL7
|GENE_ID=9820
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.43006687G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609577.0001
|CLNSIG=5
|CLNCUI=C1848862
|CLNDBN=Three M syndrome 1
|Disease=Three M syndrome 1
|CLNACC=RCV000001680.1
|Tags=RV;PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1481:C1848862:273750:2616
|COMMON=0
}}