List of variants in gene MCCC2 reported as benign by Pars Genome Lab

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

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_022132.5(MCCC2):c.1368A>G (p.Ala456=)	rs10064079	0.82429
NM_022132.5(MCCC2):c.738+36G>A	rs12516456	0.80304
NM_022132.5(MCCC2):c.1575-64A>G	rs7443786	0.69711
NM_022132.5(MCCC2):c.803+71C>T	rs277981	0.41735
NM_022132.5(MCCC2):c.739-92G>A	rs277980	0.41731
NM_022132.5(MCCC2):c.904-12A>G	rs277984	0.30658
NM_022132.5(MCCC2):c.-117A>G	rs11746722
NM_022132.5(MCCC2):c.1488+103G>C	rs169406
NM_022132.5(MCCC2):c.1488+113G>A	rs182191
NM_022132.5(MCCC2):c.1489-111T>G	rs6888301
NM_022132.5(MCCC2):c.1574+73G>A	rs2242372

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.