List of variants reported as benign for Parkinson Disease, Dominant by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 20

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000345.4(SNCA):c.*893C>T	rs356165	0.53603
NM_014321.4(ORC6):c.-20T>C	rs33994299	0.33690
NM_000345.4(SNCA):c.*2108A>T	rs1045722	0.23733
NM_000345.4(SNCA):c.*2105G>A	rs3857053	0.23489
NM_000345.4(SNCA):c.*1287G>A	rs377356638	0.15186
NM_000345.4(SNCA):c.*501C>T	rs17016074	0.04776
NM_000345.4(SNCA):c.*1677C>T	rs17016072	0.04338
NM_000345.4(SNCA):c.*139T>G	rs10024743	0.00703
NM_000345.4(SNCA):c.*173G>A	rs79726680	0.00645
NM_000345.4(SNCA):c.*1896C>T	rs186189862	0.00484
NM_000345.4(SNCA):c.*593C>A	rs35101723	0.00475
NM_000345.4(SNCA):c.*1002T>G	rs182722435	0.00363
NM_000345.4(SNCA):c.*2230G>A	rs183802441	0.00323
NM_000345.4(SNCA):c.408C>T (p.Tyr136=)	rs76642636	0.00252
NM_000345.4(SNCA):c.121+11C>T	rs35135226	0.00022
NM_000345.4(SNCA):c.*894G>A	rs192179063	0.00011
NM_000345.4(SNCA):c.287A>G (p.Lys96Arg)	rs548523899	0.00003
NM_000345.4(SNCA):c.*249G>A	rs553599518	0.00001
NM_000345.4(SNCA):c.*1260CT[7]	rs5860180
NM_000345.4(SNCA):c.243A>G (p.Thr81=)	rs568436589

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.