ClinVar Miner

List of variants reported as uncertain significance for Breast-ovarian cancer, familial 2 by Pathway Genomics

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
Download table as spreadsheet
NM_000059.3(BRCA2):c.2138A>C (p.Gln713Pro) rs55816687
NM_000059.3(BRCA2):c.4436G>C (p.Ser1479Thr) rs80358678
NM_000059.3(BRCA2):c.467A>G (p.Asp156Gly) rs68071147
NM_000059.3(BRCA2):c.5035A>G (p.Thr1679Ala) rs80358728
NM_000059.3(BRCA2):c.566A>G (p.Asp189Gly) rs397507359
NM_000059.3(BRCA2):c.5982A>T (p.Gln1994His) rs587783043
NM_000059.3(BRCA2):c.6257T>C (p.Ile2086Thr) rs587783042
NM_000059.3(BRCA2):c.7987G>A (p.Glu2663Lys) rs80359030
NM_000059.3(BRCA2):c.8087T>G (p.Leu2696Trp) rs80359050
NM_000059.3(BRCA2):c.8423T>C (p.Leu2808Pro) rs587783044

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.