{{Rsnum
|rsid=121434585
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GNAT2
|position=109610108
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GNAT2
}}{{omim
|id=139340
|rsnum=121434585
|variant=0001
}}{{ClinVar
|rsid=121434585
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=109610108
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000605000002110100
|GENEINFO=GNAT2:2780
|GENE_NAME=GNAT2
|GENE_ID=2780
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.109610108G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_005272.3:c.235C>T; 139340.0001
|CLNSIG=5
|CLNCUI=C1841721
|CLNDBN=Achromatopsia 4
|Disease=Achromatopsia 4
|CLNACC=RCV000017273.22
|Tags=RV;PM;S3D;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1418:C1841721:613856:ORPHA49382
}}