ClinVar Miner

List of variants in gene PLA2G6 studied for Parkinson disease

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP
NM_003560.4(PLA2G6):c.101C>T (p.Ser34Leu) rs147948449
NM_003560.4(PLA2G6):c.1354C>T (p.Gln452Ter) rs387906864
NM_003560.4(PLA2G6):c.1427+1G>A rs750939090
NM_003560.4(PLA2G6):c.1615G>A (p.Gly539Ser) rs143826762
NM_003560.4(PLA2G6):c.16C>T (p.Arg6Cys) rs143250889
NM_003560.4(PLA2G6):c.1904G>A (p.Arg635Gln) rs387906863
NM_003560.4(PLA2G6):c.216C>A (p.Phe72Leu)
NM_003560.4(PLA2G6):c.2222G>A (p.Arg741Gln) rs121908686
NM_003560.4(PLA2G6):c.2239C>T (p.Arg747Trp) rs121908687
NM_003560.4(PLA2G6):c.2370T>G (p.Tyr790Ter) rs121908680
NM_003560.4(PLA2G6):c.238G>A (p.Ala80Thr) rs121908685
NM_003560.4(PLA2G6):c.416G>A (p.Arg139His) rs141825182
NM_003560.4(PLA2G6):c.898G>A (p.Ala300Thr) rs528966598
NM_003560.4(PLA2G6):c.91G>A (p.Asp31Asn) rs150024227
NM_003560.4(PLA2G6):c.991G>T (p.Asp331Tyr) rs199935023

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.