{{Rsnum
|rsid=104893628
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CYP1B1
|position=38074695
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP1B1
}}{{omim
|id=601771
|rsnum=104893628
|variant=0013
}}{{ClinVar
|rsid=104893628
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=38301838
|CHROM=2
|dbSNPBuildID=137
|SSR=0
|SAO=0
|VP=0x050260000000000002110100
|GENEINFO=CYP1B1:1545
|GENE_NAME=CYP1B1
|GENE_ID=1545
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.38301838C>G
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601771.0013
|CLNSIG=5
|CLNCUI=C0020302
|CLNDBN=Glaucoma, congenital
|Disease=Glaucoma
|CLNACC=RCV000008179.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1135:C0020302:231300
}}