{{Rsnum
|rsid=62637037
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NYX
|position=41474502
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NYX
}}{{omim
|id=300278
|rsnum=62637037
|variant=0002
}}

{{ClinVar
|rsid=62637037
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=41333755
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=NYX:60506
|GENE_NAME=NYX
|GENE_ID=60506
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.41333755G>A
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=300278.0002; RISN-NYX:c.1049G>A
|CLNSIG=5
|CLNCUI=C1839601
|CLNDBN=Congenital stationary night blindness, type 1A; not provided
|Disease=Congenital stationary night blindness; not provided
|CLNACC=RCV000012174.10; RCV000086260.1
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1245:C1839601:310500:215
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}