Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs879255257
rs879255257
Entrez Id: 4882
Gene Symbol: NPR2
NPR2
CUI: C1864356
Disease:
ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE
A 0.700 CausalMutation CLINVAR