Disease: Robinow syndrome, autosomal recessive ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs863223291
rs863223291
Entrez Id: 4920
Gene Symbol: ROR2
ROR2
CUI: C1849334
Disease:
Robinow syndrome, autosomal recessive 		C 0.700 CausalMutation CLINVAR