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{{omim |id=600053 |rsnum=104893612 |variant=0001 }}{{ClinVar |rsid=104893612 |Reversed=0 |FwdREF=C |FwdALT=T |REF=C |ALT=T |RSPOS=99006159 |CHROM=2 |dbSNPBuildID=132 |SSR=0 |SAO=1 |VP=050060000a01000002110100 |GENEINFO=CNGA3:1261 |GENE_NAME=CNGA3 |GENE_ID=1261 |WGT=1 |VC=SNV |CLNALLE=1 |CLNHGVS=NC_000002.11:g.99006159C>T |CLNSRC=OMIM Allelic Variant |CLNORIGIN=1 |CLNSRCID=600053.0001 |CLNSIG=5 |CLNCUI=C0302129 |CLNDBN=Rod monochromacy |Disease=Rod monochromacy |CLNACC=SCV000030302.1 |Tags=PM;NSM;REF;OTHERKG;LSD;OM }}
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