{{Rsnum
|rsid=122456133
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CACNA1F
|position=49228048
|Gene_s=CACNA1F
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300110
|variant=0001
|rsnum=122456133
}}{{ClinVar
|rsid=122456133
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=49084510
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CACNA1F:778
|GENE_NAME=CACNA1F
|GENE_ID=778
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.49084510C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300110.0001
|CLNSIG=5
|CLNCUI=C1848172
|CLNDBN=Congenital stationary night blindness, type 2A
|Disease=Congenital stationary night blindness
|CLNACC=RCV000012380.21
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=295317:NBK1245:C1848172:300071:215
}}