{{Rsnum
|rsid=104894114
|Chromosome=9
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=KCNV2
|position=2718655
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
}}{{omim
|id=607604
|rsnum=104894114
|variant=0002
}}{{ClinVar
|rsid=104894114
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=2718655
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=KCNV2:169522
|GENE_NAME=KCNV2
|GENE_ID=169522
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.2718655G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607604.0002
|CLNSIG=5
|CLNCUI=C1835897
|CLNDBN=Retinal cone dystrophy 3B
|Disease=Retinal cone dystrophy 3B
|CLNACC=RCV000003147.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1835897:610356:209932
}}