{{Rsnum
|rsid=75267011
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CNNM4
|position=96761706
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CNNM4
}}{{omim
|id=607805
|rsnum=75267011
|variant=0002
}}{{ClinVar
|rsid=75267011
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=97427443
|CHROM=2
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CNNM4:26504
|GENE_NAME=CNNM4
|GENE_ID=26504
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.97427443G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=607805.0002
|CLNSIG=5
|CLNCUI=C1857588
|CLNDBN=Cone-rod dystrophy amelogenesis imperfecta
|Disease=Cone-rod dystrophy amelogenesis imperfecta
|CLNACC=RCV000002982.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1857588:217080:1873
}}