{{Rsnum
|rsid=140256288
|Chromosome=9
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNV2
|position=2718181
|Gene_s=KCNV2
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=A,T
|CHROM=9
|CLNACC=RCV000033032.1
|CLNALLE=2
|CLNDBN=Retinal cone dystrophy 3B
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1835897:610356:209932
|CLNHGVS=NC_000009.11:g.2718181G>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607604.0009
|Disease=Retinal cone dystrophy 3B
|FwdALT=A,T
|FwdREF=G
|GENEINFO=KCNV2:169522
|GENE_ID=169522
|GENE_NAME=KCNV2
|REF=G
|RSPOS=2718181
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=134
|rsid=140256288
}}