{{Rsnum
|rsid=122456135
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CACNA1F
|position=49219344
|Gene_s=CACNA1F
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300110
|variant=0004
|rsnum=122456135
}}{{ClinVar
|rsid=122456135
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=49075803
|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.49075803G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300110.0004
|CLNSIG=5
|CLNCUI=C1848172
|CLNDBN=Congenital stationary night blindness, type 2A
|Disease=Congenital stationary night blindness
|CLNACC=RCV000012383.15
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=295317:NBK1245:C1848172:300071:215
}}