{{Rsnum
|rsid=137852296
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GPR143
|position=9759390
|Gene_s=GPR143
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300808
|variant=0003
|rsnum=137852296
}}
{{omim
|id=300808
|variant=0006
|rsnum=137852296
}}{{ClinVar
|rsid=137852296
|Reversed=1
|FwdREF=T
|FwdALT=A,C
|REF=A
|ALT=G,T
|RSPOS=9727430
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=GPR143:4935
|GENE_NAME=GPR143
|GENE_ID=4935
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000023.10:g.9727430A>G; NC_000023.10:g.9727430A>T
|CLNORIGIN=1
|CLNSRCID=
300808.0003; RISN-OA1:c.397T>C; 300808.0006; RISN-OA1:c.397T>A
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000011262.6; RCV000084931.1; RCV000011265.3; RCV000084930.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDBN=Ocular albinism, type I; not provided
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=20301517:NBK1343:C0342684:300500:54:78642008
|CLNSRC=OMIM Allelic Variant; Retina International
|Disease=Ocular albinism; not provided
}}