{{Rsnum
|rsid=387906826
|Chromosome=1
|position=52397707
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ORC1
|Gene_s=ORC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=1
|CLNACC=RCV000023154.1
|CLNALLE=1
|CLNDBN=Meier-Gorlin syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1868684:224690:ORPHA2554
|CLNHGVS=NC_000001.11:g.52397707T>C
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_004153.3:c.380A>G; 601902.0001
|Disease=Meier-Gorlin syndrome
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=52397707
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=387906826
|GENEINFO=ORC1:4998
|GENE_ID=4998
|GENE_NAME=ORC1
|CLNORIGIN=1
}}