{{Rsnum
|rsid=121434621
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=OPN1LW
|position=154154602
|Gene_s=OPN1LW
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121434621
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=153420077
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=OPN1LW:5956
|GENE_NAME=OPN1LW
|GENE_ID=5956
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153420077T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300822.0003
|CLNSIG=5
|CLNCUI=C0339537
|CLNDBN=Cone monochromatism
|Disease=Cone monochromatism
|CLNACC=RCV000011251.4
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0339537:303700:16:24704003
}}