List of variants reported as likely benign for Fanconi anemia complementation group O by Mendelics

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.572-17G>T	rs193023469	0.00513
NM_058216.3(RAD51C):c.376G>A (p.Ala126Thr)	rs61758784	0.00349
NM_058216.3(RAD51C):c.146-8A>G	rs201079501	0.00074
NM_058216.3(RAD51C):c.145+12T>G	rs377297129	0.00024
NC_000017.11:g.58692541G>A	rs545213879	0.00021
NM_058216.3(RAD51C):c.1026+43C>T	rs750859385	0.00002
NM_058216.3(RAD51C):c.146-3C>T	rs765143155	0.00002
NM_058216.3(RAD51C):c.141C>T (p.Ser47=)	rs568912602	0.00001
NM_058216.3(RAD51C):c.145+11C>G	rs1263551026	0.00001
NM_058216.3(RAD51C):c.115C>T (p.Leu39=)	rs759149207
NM_058216.3(RAD51C):c.145+15T>C	rs780116924
NM_058216.3(RAD51C):c.262C>T (p.Leu88=)	rs786201383
NM_058216.3(RAD51C):c.461A>G (p.Glu154Gly)	rs758847241

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.