{{Rsnum
|rsid=397509379
|Chromosome=4
|position=109869900
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=LRIT3
|Gene_s=LRIT3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=4
|CLNACC=RCV000032635.2
|CLNALLE=1
|CLNDBN=Congenital stationary night blindness, type 1F
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN165239:615058:215
|CLNHGVS=NC_000004.11:g.110791056C>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=615004.0003
|Disease=Congenital stationary night blindness
|FwdALT=G
|FwdREF=C
|REF=C
|RSPOS=110791056
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397509379
|GENEINFO=LRIT3:345193
|GENE_ID=345193
|GENE_NAME=LRIT3
}}