{{Rsnum
|rsid=62638214
|Chromosome=5
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GRM6
|position=178986393
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GRM6
}}{{omim
|id=604096
|rsnum=62638214
|variant=0001
}}

{{ClinVar
|rsid=62638214
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=178413394
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=GRM6:2916
|GENE_NAME=GRM6
|GENE_ID=2916
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.178413394G>A
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=604096.0001; RISN-GRM6:c.1861C>T
|CLNSIG=5
|CLNCUI=C1850362
|CLNDBN=Congenital stationary night blindness, type 1B; not provided
|Disease=Congenital stationary night blindness; not provided
|CLNACC=RCV000006197.1; RCV000086036.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1850362:257270:215
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}