{{Rsnum
|rsid=74552543
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CNNM4
|position=96761970
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CNNM4
}}{{omim
|id=607805
|rsnum=74552543
|variant=0003
}}{{ClinVar
|rsid=74552543
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=97427707
|CHROM=2
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=CNNM4:26504
|GENE_NAME=CNNM4
|GENE_ID=26504
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.97427707T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607805.0003
|CLNSIG=5
|CLNCUI=C1857588
|CLNDBN=Cone-rod dystrophy amelogenesis imperfecta
|Disease=Cone-rod dystrophy amelogenesis imperfecta
|CLNACC=RCV000002983.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1857588:217080:1873
}}{{PMID Auto
|PMID=19200525
|Title=Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta.
|OA=1
}}