{{Rsnum
|rsid=281875234
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GPR179
|position=38334016
|Gene_s=GPR179
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=17
|CLNACC=RCV000024199.1; RCV000059653.1
|CLNALLE=1
|CLNDBN=Congenital stationary night blindness, type 1E; not provided
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3281215:614565:215
|CLNHGVS=NC_000017.10:g.36489899G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=614515.0001; VAR_067928
|Disease=Congenital stationary night blindness; not provided
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=36489899
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050168000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=281875234
|GENEINFO=GPR179:440435
|GENE_ID=440435
|GENE_NAME=GPR179
}}{{PMID Auto
|PMID=22325361
|Title=Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.
|OA=1
}}