{{Rsnum
|rsid=145415848
|Chromosome=15
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CIB2
|position=78111171
|Gene_s=CIB2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G,T
|CAF=0.9995; 0.0004591
|CHROM=15
|CLNACC=RCV000032890.2
|CLNALLE=1
|CLNDBN=Usher syndrome, type 1J
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1265:CN158799:614869:231169:886
|CLNHGVS=NC_000015.9:g.78403513C>G
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1265; 605564.0004
|COMMON=0
|Disease=Usher syndrome
|FwdALT=G,T
|FwdREF=C
|GENEINFO=CIB2:10518
|GENE_ID=10518
|GENE_NAME=CIB2
|REF=C
|RSPOS=78403513
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000016110100
|WGT=0
|dbSNPBuildID=134
|rsid=145415848
}}