{{Rsnum
|rsid=104894915
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=OPN1MW
|position=154187939
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OPN1MW
}}{{omim
|id=300821
|rsnum=104894915
|variant=0003
}}{{ClinVar
|rsid=104894915
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=153453428
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=OPN1MW:2652
|GENE_NAME=OPN1MW
|GENE_ID=2652
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153453428C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300821.0003
|CLNSIG=5
|CLNCUI=C0155016
|CLNDBN=Colorblindness, partial, deutan series
|Disease=Colorblindness
|CLNACC=RCV000011258.6
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1301:C0155016:303800
}}