{{Rsnum
|rsid=121434304
|Chromosome=5
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GRM6
|position=178989075
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GRM6
}}{{omim
|id=604096
|rsnum=121434304
|variant=0008
}}{{ClinVar
|rsid=121434304
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=178416076
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GRM6:2916
|GENE_NAME=GRM6
|GENE_ID=2916
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.178416076A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604096.0008
|CLNSIG=5
|CLNCUI=C1850362
|CLNDBN=Congenital stationary night blindness, type 1B
|Disease=Congenital stationary night blindness
|CLNACC=RCV000006204.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1850362:257270:215
}}