{{Rsnum
|rsid=104893740
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GNAT1
|position=50193139
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GNAT1
}}{{omim
|id=139330
|rsnum=104893740
|variant=0001
}}{{ClinVar
|rsid=104893740
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=50230572
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GNAT1:2779
|GENE_NAME=GNAT1
|GENE_ID=2779
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.50230572G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=139330.0001
|CLNSIG=5
|CLNCUI=C1864870
|CLNDBN=Congenital stationary night blindness, autosomal dominant 3
|Disease=Congenital stationary night blindness
|CLNACC=RCV000017277.26
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1864870:610444:215
}}