{{Rsnum
|rsid=61748559
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ABCA4
|position=94063157
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ABCA4
}}{{omim
|id=601691
|rsnum=61748559
|variant=0022
}}{{ClinVar
|rsid=61748559
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=94063157
|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; 2
|CLNHGVS=NC_000001.11:g.94063157C>G; NC_000001.11:g.94063157C>T
|CLNSRC=ClinVar; Retina International; OMIM Allelic Variant
|CLNORIGIN=0; 1
|CLNSRCID=NM_000350.2:c.1715G>C; RISN-ABCR:c.1715G>C; NM_000350.2:c.1715G>A; 601691.0022; RISN-ABCR:c.1715G>A
|CLNSIG=5
|CLNCUI=C1855465
|CLNDBN=not provided; Stargardt disease 1
|Disease=not provided; Stargardt disease 1
|CLNACC=RCV000085417.1; RCV000008357.2; RCV000085416.1
|Tags=RV;PM;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1855465:248200:ORPHA827
}}