ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.336C>T (p.Gly112=)

dbSNP: rs2142436504
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV004574678 SCV006095468 benign Breast-ovarian cancer, familial, susceptibility to, 4 2025-02-21 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.
Baylor Genetics RCV004574678 SCV005054041 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 4 2023-11-20 criteria provided, single submitter clinical testing

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. The submitted information has not been verified. If you have questions about the information contained on this website, please see a health care professional.