{{Rsnum
|rsid=121909086
|Chromosome=9
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ROR2
|position=91737400
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ROR2
}}{{omim
|id=602337
|rsnum=121909086
|variant=0007
}}{{ClinVar
|rsid=121909086
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=94499682
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ROR2:4920
|GENE_NAME=ROR2
|GENE_ID=4920
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.94499682G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602337.0007
|CLNSIG=5
|CLNCUI=C1849334
|CLNDBN=Robinow syndrome, autosomal recessive
|Disease=Robinow syndrome
|CLNACC=RCV000007733.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1240:C1849334:268310:1507:97360
}}