NRP2, neuropilin 2, 8828

N. diseases: 144; N. variants: 4
Disease: Multiple congenital anomalies ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs779617179
rs779617179
Entrez Id: 8828
Gene Symbol: NRP2
NRP2
CUI: C0000772
Disease:
Multiple congenital anomalies 		C 0.700 GeneticVariation CLINVAR