{{Rsnum
|rsid=397514604
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KCNV2
|position=2718230
|Gene_s=KCNV2
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=C
|CHROM=9
|CLNACC=RCV000033033.1
|CLNALLE=1
|CLNDBN=Retinal cone dystrophy 3B
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1835897:610356:209932
|CLNHGVS=NC_000009.11:g.2718230T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607604.0010
|Disease=Retinal cone dystrophy 3B
|FwdALT=C
|FwdREF=T
|GENEINFO=KCNV2:169522
|GENE_ID=169522
|GENE_NAME=KCNV2
|REF=T
|RSPOS=2718230
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514604
}}