{{Rsnum
|rsid=62637014
|Gene=AIPL1
|Chromosome=17
|position=6425781
|Orientation=minus
|GMAF=0.0
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=AIPL1
}}{{omim
|id=604392
|rsnum=62637014
|variant=0001
}}

{{PMID Auto
|PMID=22412862
|Title=Leber Congenital Amaurosis Associated with AIPL1: Challenges in Ascribing Disease Causation, Clinical Findings, and Implications for Gene Therapy
|OA=1
}}
{{ClinVar
|rsid=62637014
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=6329101
|CHROM=17
|GMAF=0
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000040016110100
|GENEINFO=AIPL1:23746
|GENE_NAME=AIPL1
|GENE_ID=23746
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.6329101C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=NBK1298; 604392.0001; RISN-AIPL1:c.834G>A
|CLNSIG=5
|CLNCUI=C1858386
|CLNDBN=Leber congenital amaurosis 4; not provided
|Disease=Leber congenital amaurosis 4; not provided
|CLNACC=RCV000005906.2; RCV000086235.1
|Tags=RV;PM;S3D;SLO;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=1; 0
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1298:C1858386:604393
|COMMON=0
}}

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