{{Rsnum
|rsid=80359870
|Chromosome=X
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=CACNA1F
|position=49216484
|Gene_s=CACNA1F
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=AG
|CHROM=X
|CLNACC=RCV000020629.2
|CLNALLE=1
|CLNDBN=Congenital stationary night blindness, type 2A
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=295317:NBK1245:C1848172:300071:215
|CLNHGVS=NC_000023.10:g.49072945dupG
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1245
|Disease=Congenital stationary night blindness
|FwdALT=C
|GENEINFO=CACNA1F:778
|GENE_ID=778
|GENE_NAME=CACNA1F
|REF=A
|RSPOS=49072944
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=132
|rsid=80359870
}}{{PMID Auto
|PMID=9662400
|Title=Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
}}

{{PMID Auto
|PMID=10900517
|Title=Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F.
}}