{{Rsnum
|rsid=61751392
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ABCA4
|position=94063250
|Gene_s=ABCA4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=61751392
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=94063250
|CHROM=1
|dbSNPBuildID=134
|SSR=0
|SAO=0
|VP=0x050160000a05040002110100
|GENEINFO=ABCA4:24
|GENE_NAME=ABCA4
|GENE_ID=24
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.94063250A>G
|CLNSRC=ClinVar; OMIM Allelic Variant; Retina International
|CLNSRCID=NM_000350.2:c.1622T>C; 601691.0023; RISN-ABCR:c.1622T>C
|CLNSIG=5
|CLNCUI=C1855465; C1858806
|CLNDBN=Stargardt disease 1; Cone-rod dystrophy 3; not provided
|Disease=Stargardt disease 1; Cone-rod dystrophy 3; not provided
|CLNACC=RCV000008358.2; RCV000008359.2; RCV000085410.1
|Tags=RV;PM;SLO;NSM;REF;ASP;VLD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1855465:248200:ORPHA827; C1858806:604116:ORPHA1872
|CLNORIGIN=1
}}

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