{{Rsnum
|rsid=121909206
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=ABCA4
|position=94015766
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ABCA4
}}{{omim
|id=601691
|rsnum=121909206
|variant=0031
}}{{ClinVar
|rsid=121909206
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=94015766
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=ABCA4:24
|GENE_NAME=ABCA4
|GENE_ID=24
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.94015766G>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000350.2:c.5285C>A; 601691.0031
|CLNSIG=5
|CLNCUI=C1858806; C1855465
|CLNDBN=Cone-rod dystrophy 3; Stargardt disease 1
|Disease=Cone-rod dystrophy 3; Stargardt disease 1
|CLNACC=RCV000008367.1; RCV000008368.2
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1858806:604116:ORPHA1872; C1855465:248200:ORPHA827
}}