{{Rsnum
|rsid=121909205
|Gene=ABCA4
|Chromosome=1
|position=94120994
|Orientation=minus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ABCA4
}}{{omim
|id=601691
|rsnum=121909205
|variant=0021
}}{{ClinVar
|rsid=121909205
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=94120994
|CHROM=1
|GMAF=0.0009
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000a05040016110100
|GENEINFO=ABCA4:24
|GENE_NAME=ABCA4
|GENE_ID=24
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.94120994G>A
|CLNSRC=ClinVar; OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=NM_000350.2:c.52C>T; 601691.0021; RISN-ABCR:c.52C>T
|CLNSIG=5
|CLNCUI=C1855465
|CLNDBN=Stargardt disease 1; not provided
|Disease=Stargardt disease 1; not provided
|CLNACC=RCV000008356.1; RCV000085719.1
|Tags=RV;PM;SLO;NSM;REF;ASP;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1855465:248200:ORPHA827
|COMMON=1
}}