{{Rsnum
|rsid=121909085
|Chromosome=9
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ROR2
|position=91724334
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ROR2
}}{{omim
|id=602337
|rsnum=121909085
|variant=0006
}}{{ClinVar
|rsid=121909085
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=94486616
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ROR2:4920
|GENE_NAME=ROR2
|GENE_ID=4920
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.94486616C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602337.0006
|CLNSIG=5
|CLNCUI=C1849334
|CLNDBN=Robinow syndrome, autosomal recessive
|Disease=Robinow syndrome
|CLNACC=RCV000007732.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1240:C1849334:268310:1507:97360
}}