{{Rsnum
|rsid=121917828
|Gene=CABP4
|Chromosome=11
|position=67456191
|Orientation=plus
|GMAF=0.0004591
|Gene_s=CABP4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|rsid=121917828
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=67223662
|CHROM=11
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=CABP4:57010
|GENE_NAME=CABP4
|GENE_ID=57010
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.67223662C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608965.0002
|CLNSIG=5
|CLNCUI=C1864877
|CLNDBN=Congenital stationary night blindness, type 2B
|Disease=Congenital stationary night blindness
|CLNACC=RCV000002030.1
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1864877:610427:215
|COMMON=0
}}