List of variants studied for Autosomal recessive Parkinson disease 14

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003560.4(PLA2G6):c.2417C>G (p.Pro806Arg)	rs140758033	0.00046
NM_003560.4(PLA2G6):c.956C>T (p.Thr319Met)	rs149653983	0.00029
NM_003560.4(PLA2G6):c.2222G>A (p.Arg741Gln)	rs121908686	0.00009
NM_003560.4(PLA2G6):c.2239C>T (p.Arg747Trp)	rs121908687	0.00003
NM_003560.4(PLA2G6):c.1061T>C (p.Leu354Pro)	rs1403125636	0.00001
NM_003560.4(PLA2G6):c.1354C>T (p.Gln452Ter)	rs387906864
NM_003560.4(PLA2G6):c.1634A>C (p.Lys545Thr)	rs121908681
NM_003560.4(PLA2G6):c.1904G>A (p.Arg635Gln)	rs387906863
NM_003560.4(PLA2G6):c.216C>A (p.Phe72Leu)	rs774631197
NM_003560.4(PLA2G6):c.29C>A (p.Thr10Asn)	rs1323819447
NM_003560.4(PLA2G6):c.797G>C (p.Gly266Ala)	rs764286950
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.