{{Rsnum
|rsid=62637027
|Chromosome=X
|Orientation=plus
|geno1=(AA;AA)
|geno2=(AA;GC)
|geno3=(GC;GC)
|Gene=NYX
|position=41474012
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NYX
}}{{omim
|id=300278
|rsnum=62637027
|variant=0004
}}{{ClinVar
|rsid=62637027
|Reversed=0
|FwdREF=GC
|FwdALT=AA
|REF=CGC
|ALT=CAA
|RSPOS=41333264
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110800
|GENEINFO=NYX:60506
|GENE_NAME=NYX
|GENE_ID=60506
|WGT=0
|VC=MNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.41333265_41333266delGCinsAA
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300278.0004
|CLNSIG=5
|CLNCUI=C1839601
|CLNDBN=Congenital stationary night blindness, type 1A; not provided
|Disease=Congenital stationary night blindness; not provided
|CLNACC=RCV000012176.10; RCV000086268.1
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1245:C1839601:310500:215
}}