Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912739
rs121912739
Entrez Id: 4882
Gene Symbol: NPR2
NPR2
CUI: C1864356
Disease:
ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE
T 0.700 CausalMutation CLINVAR