List of variants in gene PACRG, PRKN studied for autosomal recessive juvenile Parkinson disease 2

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004562.3(PRKN):c.-30T>C	rs200065081	0.00671
NM_004562.3(PRKN):c.-42T>C	rs112850281	0.00042
NM_004562.3(PRKN):c.-46C>T	rs369389244	0.00011
NM_004562.3(PRKN):c.2T>C (p.Met1Thr)	rs771586218	0.00008
NM_004562.3(PRKN):c.-85G>A	rs556535340	0.00004
NM_004562.3(PRKN):c.-57G>C	rs750626864	0.00001
NC_000006.11:g.(162683798_162864341)_(162864506_163148693)dup
NM_004562.3(PRKN):c.-78C>A	rs765761156
NM_004562.3(PRKN):c.7+1G>T	rs397518439
NM_004562.3(PRKN):c.7+4C>T	rs749081702

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.