{{Rsnum
|rsid = 28936701
|Gene = CYP1B1
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=2
|position=38070949
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP1B1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 99.1 | 0.9 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=GLAUCOMA 3, PRIMARY CONGENITAL, A
|id=601771
|rsnum=28936701
|variant=0006
}}

{{ neighbor
| rsid = 1056836
| distance = 111
}}

{{ClinVar
|rsid=28936701
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=38298092
|CHROM=2
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000000402110100
|GENEINFO=CYP1B1:1545
|GENE_NAME=CYP1B1
|GENE_ID=1545
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.38298092G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601771.0006
|CLNSIG=5
|CLNCUI=C0020302
|CLNDBN=Glaucoma, congenital
|Disease=Glaucoma
|CLNACC=RCV000008172.1
|Tags=RV;PM;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1135:C0020302:231300
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}