{{Rsnum
|rsid=368062092
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=NMNAT1
|position=9982571
|Gene_s=NMNAT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|RSPOS=9982571
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNACC=RCV000030769.1
|CLNDBN=Leber congenital amaurosis 9
|dbSNPBuildID=137
|FwdALT=T
|REF=G
|CLNSRC=ClinVar; OMIM Allelic Variant
|SAO=0
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|Reversed=0
|rsid=368062092
|CLNALLE=1
|CHROM=1
|VC=SNV
|Disease=Leber congenital amaurosis 9
|VP=0x050260000a05000002110100
|WGT=1
|FwdREF=G
|CLNDSDBID=NBK1298:C1837873:608553:ORPHA65
|SSR=0
|CLNHGVS=NC_000001.11:g.9982571G>T
|ALT=T
|CLNSIG=5
|CLNSRCID=NM_022787.3:c.710G>T; 608700.0007
|GENEINFO=NMNAT1:64802
|GENE_ID=64802
|GENE_NAME=NMNAT1
|CLNORIGIN=1
}}