Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553456695
rs1553456695
Entrez Id: 4929
Gene Symbol: NR4A2
NR4A2
CUI: C0014544
Disease:
Epilepsy
AC 0.700 GeneticVariation CLINVAR
dbSNP: rs35479735
rs35479735
Entrez Id: 4929
Gene Symbol: NR4A2
NR4A2
CUI: C0030567
Disease:
Parkinson Disease
0.020 GeneticVariation BEFREE The rs35479735 polymorphism was associated with a higher risk of developing PD. 28716280 2017
dbSNP: rs35479735
rs35479735
Entrez Id: 4929
Gene Symbol: NR4A2
NR4A2
CUI: C0030567
Disease:
Parkinson Disease
0.020 GeneticVariation BEFREE The study comprehensively evaluated the association of NR4A2 variation with PD, and the results failed to demonstrate that the NR4A2 polymorphisms significantly associated with PD except for rs35479735, suggesting that more studies are needed to elucidate if NR4A2 is a risk of PD. 28385514 2017
dbSNP: rs1453063924
rs1453063924
Entrez Id: 4929
Gene Symbol: NR4A2
NR4A2
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study. 15966003 2005