ClinVar Miner

List of variants reported as uncertain significance for BAP1-related tumor predisposition syndrome by Ambry Genetics

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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NM_000535.7(PMS2):c.1438G>C (p.Gly480Arg) rs146848345
NM_032043.2(BRIP1):c.262_264delTGT rs587781388

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