{{Rsnum
|rsid=140287375
|Chromosome=14
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SPATA7
|position=88416725
|Gene_s=SPATA7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=14
|CLNACC=RCV000023791.1
|CLNALLE=1
|CLNDBN=Leber congenital amaurosis 3
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1298:C1858677:604232
|CLNHGVS=NC_000014.8:g.88883069C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=609868.0007
|Disease=Leber congenital amaurosis 3
|FwdALT=T
|FwdREF=C
|GENEINFO=SPATA7:55812
|GENE_ID=55812
|GENE_NAME=SPATA7
|REF=C
|RSPOS=88883069
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=134
|rsid=140287375
}}