{{Rsnum
|rsid=28937873
|Gene=NR2E3
|Chromosome=15
|position=71813573
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.001837
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=NR2E3
}}{{omim
|desc=ENHANCED S-CONE SYNDROME
|id=604485
|rsnum=28937873
|variant=0005
}}

{{ClinVar
|rsid=28937873
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=72105913
|CHROM=15
|GMAF=0.0018
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000016110100
|GENEINFO=NR2E3:10002
|GENE_NAME=NR2E3
|GENE_ID=10002
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.72105913G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604485.0005
|CLNSIG=5
|CLNCUI=C1849394
|CLNDBN=Enhanced s-cone syndrome; Goldmann-Favre syndrome
|Disease=Enhanced s-cone syndrome; Goldmann-Favre syndrome
|CLNACC=RCV000005869.1; RCV000005870.1
|Tags=PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9982; 0.001837
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=C1849394:268100:53540; C0339541
|COMMON=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}