{{Rsnum
|rsid=104894911
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NYX
|position=41473755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NYX
}}{{omim
|id=300278
|rsnum=104894911
|variant=0006
}}{{ClinVar
|rsid=104894911
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=41333008
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NYX:60506
|GENE_NAME=NYX
|GENE_ID=60506
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.41333008T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300278.0006
|CLNSIG=5
|CLNCUI=C1839601
|CLNDBN=Congenital stationary night blindness, type 1A
|Disease=Congenital stationary night blindness
|CLNACC=RCV000012178.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1245:C1839601:310500:215
}}