{{Rsnum
|rsid=121909762
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GPR98
|position=90690991
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GPR98
}}{{omim
|id=602851
|rsnum=121909762
|variant=0002
}}{{ClinVar
|rsid=121909762
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=89986808
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GPR98:84059
|GENE_NAME=GPR98
|GENE_ID=84059
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.89986808C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602851.0002
|CLNSIG=5
|CLNCUI=C1854237
|CLNDBN=Usher syndrome, type 2C
|Disease=Usher syndrome
|CLNACC=RCV000007200.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1341:C1854237:605472:231178:886
}}