{{Rsnum
|rsid = 713
|Gene=OPN1LW
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=X
|position=154152987
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{Venter SNP
|rsid=713
|allele=A
|frequency=
|uid=1103673116349
|type=homozygous_SNP
|hugo=OPN1LW
|ensembl gene=ENSG00000102076
|ensembl transcript=ENST00000369951
|sift=TOLERATED
|disease=Defects in OPN1LW are the cause of partial colorblindness protan series (CBP) (MIM:303900); also called protanopia.
}}

{{GET Evidence
|gene=OPN1LW
|aa_change=Leu153Met
|aa_change_short=L153M
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs713
|overall_frequency_n=97
|overall_frequency_d=8030
|overall_frequency=0.0120797
|n_genomes=9
|n_genomes_annotated=0
|n_haplomes=18
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=-3
|autoscore=3
|webscore=N
}}
{{on chip | HumanOmni1Quad}}