NRP1, neuropilin 1, 8829

N. diseases: 246; N. variants: 13
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10080
rs10080
Entrez Id: 8829
Gene Symbol: NRP1
NRP1
CUI: C0039685
Disease:
Tetralogy of Fallot
0.010 GeneticVariation BEFREE In addition, the association analysis suggested for the first time that there is a strong association between the allele distribution of rs10080 and susceptibility to TOF (p = 0.001). 29432830 2018