ClinVar Miner

List of variants in gene NR4A2 studied for Parkinson disease

Included ClinVar conditions (41):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006186.4(NR4A2):c.*331T>G rs12803 0.39211
NM_006186.4(NR4A2):c.*352C>A rs115393922 0.00316
NM_006186.4(NR4A2):c.732C>A (p.Leu244=) rs16840266 0.00110
NM_006186.4(NR4A2):c.*1249A>G rs564495914 0.00049
NM_006186.4(NR4A2):c.*933G>A rs563505935 0.00025
NM_006186.4(NR4A2):c.585C>T (p.Asp195=) rs143064317 0.00017
NM_006186.4(NR4A2):c.-339C>A rs1055625772 0.00016
NM_006186.3(NR4A2):c.*1311A>G rs886054974 0.00015
NM_006186.4(NR4A2):c.*192C>G rs747113198 0.00007
NM_006186.4(NR4A2):c.1158+13C>T rs372468197 0.00007
NM_006186.4(NR4A2):c.360T>G (p.Val120=) rs201399912 0.00006
NM_006186.4(NR4A2):c.657T>C (p.Ala219=) rs769677341 0.00006
NM_006186.4(NR4A2):c.1163A>T (p.Gln388Leu) rs767330388 0.00004
NM_006186.4(NR4A2):c.-325C>G rs886054981 0.00003
NM_006186.4(NR4A2):c.1659C>G (p.Ser553=) rs886054977 0.00003
NM_006186.4(NR4A2):c.1746G>A (p.Val582=) rs886054976 0.00003
NM_006186.3(NR4A2):c.-384T>C rs886054982 0.00002
NM_006186.4(NR4A2):c.*1198C>T rs577905348 0.00002
NM_006186.4(NR4A2):c.*1017T>C rs986511917 0.00001
NM_006186.4(NR4A2):c.*599T>G rs1268567400 0.00001
NM_006186.4(NR4A2):c.1230G>A (p.Leu410=) rs139491338 0.00001
NM_006186.4(NR4A2):c.1273C>T (p.Pro425Ser) rs371624401 0.00001
NM_006186.4(NR4A2):c.1548C>T (p.His516=) rs1343095735 0.00001
NM_006186.4(NR4A2):c.325C>G (p.Gln109Glu) rs747551776 0.00001
NM_006186.4(NR4A2):c.372C>T (p.Pro124=) rs943205037 0.00001
NM_006186.3(NR4A2):c.-437A>G rs1686993973
NM_006186.4(NR4A2):c.*822A>C rs886054975
NM_006186.4(NR4A2):c.1170C>A (p.Asn390Lys) rs1486481129
NM_006186.4(NR4A2):c.1588A>C (p.Lys530Gln) rs1686624142
NM_006186.4(NR4A2):c.1635G>T (p.Gly545=) rs886054978
NM_006186.4(NR4A2):c.1638G>A (p.Leu546=) rs528222526
NM_006186.4(NR4A2):c.325C>A (p.Gln109Lys) rs747551776
NM_006186.4(NR4A2):c.591C>A (p.Pro197=) rs769738246
NM_006186.4(NR4A2):c.881dup (p.Asn294fs) rs1686760554
NM_006186.4(NR4A2):c.896G>T (p.Cys299Phe) rs2105605264

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.