ClinVar Miner

List of variants reported as uncertain significance by MVZ Praenatalmedizin und Genetik Nuernberg

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP
NM_000051.3(ATM):c.6198+11T>C rs774664615
NM_000059.3(BRCA2):c.1129G>C (p.Glu377Gln) rs876658625
NM_000059.3(BRCA2):c.474A>G (p.Ser158=) rs886041101
NM_000059.3(BRCA2):c.9311A>G (p.Lys3104Arg) rs956554593
NM_004360.5(CDH1):c.1633C>T (p.Arg545Trp) rs863224727
NM_007294.4(BRCA1):c.332A>C (p.Glu111Ala) rs80357312
NM_007294.4(BRCA1):c.3454G>A (p.Asp1152Asn) rs80357175
NM_024675.3(PALB2):c.2756T>G (p.Val919Gly) rs886041103
NM_024675.4(PALB2):c.1751ATG[4] (p.Asp586dup) rs1555460665

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.