{{Rsnum
|rsid=387906827
|Chromosome=1
|position=52397821
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ORC1
|Gene_s=ORC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=1
|CLNACC=RCV000023155.1
|CLNALLE=1
|CLNDBN=Meier-Gorlin syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1868684:224690:ORPHA2554
|CLNHGVS=NC_000001.11:g.52397821A>G
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_004153.3:c.266T>C; 601902.0002
|Disease=Meier-Gorlin syndrome
|FwdALT=C
|FwdREF=T
|REF=A
|RSPOS=52397821
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=387906827
|GENEINFO=ORC1:4998
|GENE_ID=4998
|GENE_NAME=ORC1
|CLNORIGIN=1
}}