{{Rsnum
|rsid=55989760
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CYP1B1
|position=38071195
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP1B1
}}{{omim
|id=601771
|rsnum=55989760
|variant=0008
}}
{{omim
|id=601771
|rsnum=55989760
|variant=0014
}}{{ClinVar
|rsid=55989760
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=38298338
|CHROM=2
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050360000000040502110100
|GENEINFO=CYP1B1:1545
|GENE_NAME=CYP1B1
|GENE_ID=1545
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000002.11:g.38298338C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601771.0008; 601771.0014
|CLNSIG=5
|CLNCUI=C0020302
|CLNDBN=Glaucoma, congenital
|Disease=Glaucoma
|CLNACC=RCV000008174.1
|Tags=RV;PM;S3D;SLO;VLD;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1135:C0020302:231300
}}