{{Rsnum
|rsid=143141689
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ORC1
|position=52397773
|Gene_s=ORC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=1
|CLNACC=RCV000023156.1
|CLNALLE=1
|CLNDBN=Meier-Gorlin syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1868684:224690:ORPHA2554
|CLNHGVS=NC_000001.11:g.52397773C>T
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_004153.3:c.314G>A; 601902.0003
|Disease=Meier-Gorlin syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=ORC1:4998
|GENE_ID=4998
|GENE_NAME=ORC1
|REF=C
|RSPOS=52397773
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;NSM;REF;ASP;VLD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000a05040002110100
|WGT=1
|dbSNPBuildID=134
|rsid=143141689
|CLNORIGIN=1
}}