{{Rsnum
|rsid=61753033
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ABCA4
|position=94008767
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ABCA4
}}{{omim
|id=601691
|rsnum=61753033
|variant=0033
}}

{{ClinVar
|rsid=61753033
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=94008767
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000a05000002110100
|GENEINFO=ABCA4:24
|GENE_NAME=ABCA4
|GENE_ID=24
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.94008767A>G
|CLNSRC=ClinVar; OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=NM_000350.2:c.5819T>C; 601691.0033; RISN-ABCR:c.5819T>C
|CLNSIG=5
|CLNCUI=C0271093; C1855465; C1858806
|CLNDBN=Stargardt's disease; Stargardt disease 1; Cone-rod dystrophy 3; not provided
|Disease=Stargardt's disease; Stargardt disease 1; Cone-rod dystrophy 3; not provided
|CLNACC=RCV000008370.1; RCV000008371.1; RCV000008372.2; RCV000085762.1
|Tags=RV;PM;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=C0271093:70099003; C1855465:248200:ORPHA827; C1858806:604116:ORPHA1872
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}