{{Rsnum
|rsid=104894913
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OPN1LW
|position=154158844
|Gene_s=OPN1LW
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=104894913
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=153424319
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=OPN1LW:5956
|GENE_NAME=OPN1LW
|GENE_ID=5956
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153424319G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300822.0004
|CLNSIG=5
|CLNCUI=C0155015
|CLNDBN=Protan defect
|Disease=Protan defect
|CLNACC=RCV000011252.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1301:C0155015:303900:51445007
}}