List of variants in gene RAD51C reported by University of Washington Department of Laboratory Medicine, University of Washington

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.904+1374A>G	rs117829161	0.00841
NM_058216.3(RAD51C):c.572-17G>T	rs193023469	0.00513
NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser)	rs147241704	0.00207
NM_058216.3(RAD51C):c.966-3587A>G	rs184184551	0.00198
NM_058216.3(RAD51C):c.965+139A>G	rs768644225	0.00111
NM_058216.3(RAD51C):c.966-3595A>G	rs543996973	0.00035
NM_058216.3(RAD51C):c.706-426T>C	rs757386460	0.00024
NM_058216.3(RAD51C):c.1026+35T>C	rs372455350	0.00005
NM_058216.3(RAD51C):c.145+853A>G	rs77888603	0.00005
NM_058216.3(RAD51C):c.571+4A>G	rs587780257	0.00001
NM_058216.3(RAD51C):c.1026+5_1026+7del	rs587781410
NM_058216.3(RAD51C):c.965+179A>G	rs869312647
NM_058216.3(RAD51C):c.966-3481A>T	rs146511278

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.