NRP1, neuropilin 1, 8829

N. diseases: 246; N. variants: 13
Disease: Atrial Septal Defects ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2228638
rs2228638
Entrez Id: 8829
Gene Symbol: NRP1
NRP1
CUI: C0018817
Disease:
Atrial Septal Defects 		0.010 GeneticVariation BEFREE We found that rs2228638 in NRP1 on 10p11 was significantly increased the risk of TOF (OR = 1.52, 95% CI = 1.13-2.04, P = 0.006), but not in other subgroups including ASD and VSD. 24594544 2014