ClinVar Miner

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

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Total variants: 9
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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

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