List of variants reported as uncertain significance for Breast-ovarian cancer, familial, susceptibility to, 4 by Myriad Genetics, Inc.

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: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.26G>C (p.Cys9Ser)	rs140825795	0.00037
NM_002878.4(RAD51D):c.137C>G (p.Ser46Cys)	rs587780102	0.00010
NM_002878.4(RAD51D):c.196G>A (p.Val66Met)	rs56026142	0.00009
NM_002878.4(RAD51D):c.715C>T (p.Arg239Trp)	rs770250516	0.00006
NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys)	rs587781813	0.00004
NM_002878.4(RAD51D):c.53A>G (p.Gln18Arg)	rs546225564	0.00003
NM_002878.4(RAD51D):c.131G>A (p.Gly44Asp)	rs374730714	0.00001
NM_002878.4(RAD51D):c.286G>T (p.Gly96Cys)	rs762951311	0.00001
NM_002878.4(RAD51D):c.433C>T (p.Arg145Cys)	rs755173206	0.00001
NM_002878.4(RAD51D):c.716G>A (p.Arg239Gln)	rs780921112	0.00001
NM_002878.4(RAD51D):c.739-3C>T	rs1235042092	0.00001
NM_002878.4(RAD51D):c.339A>C (p.Lys113Asn)	rs786202507
NM_002878.4(RAD51D):c.349T>A (p.Cys117Ser)	rs786201358
NM_002878.4(RAD51D):c.785C>T (p.Pro262Leu)	rs730881950

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.