{{Rsnum
|rsid=74315331
|Chromosome=1
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MYOC
|position=171636010
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYOC
}}{{omim
|id=601652
|rsnum=74315331
|variant=0005
}}
{{omim
|id=601652
|rsnum=74315331
|variant=0017
}}{{ClinVar
|rsid=74315331
|Reversed=1
|FwdREF=T
|FwdALT=A,G
|REF=A
|ALT=C,T
|RSPOS=171636010
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=MYOC:4653
|GENE_NAME=MYOC
|GENE_ID=4653
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000001.11:g.171636010A>C; NC_000001.11:g.171636010A>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000261.1:c.1430T>G; 601652.0005; NM_000261.1:c.1430T>A; 601652.0018
|CLNCUI=C1842028,C1842028; C1842028
|CLNDBN=Primary open angle glaucoma juvenile onset 1
|Disease=Primary open angle glaucoma juvenile onset 1
|CLNACC=RCV000008413.1; RCV000023126.2
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1842028:137750:ORPHA98977
|CLNSIG=5
}}