ClinVar Miner

List of variants in gene combination BRCA2, LOC106721785 reported as benign by Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA)

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.-52A>G rs206118 0.15771
NM_000059.4(BRCA2):c.-175C>T rs55880202 0.00642
NM_000059.4(BRCA2):c.-162G>A rs567110692
NM_000059.4(BRCA2):c.-59_-57del rs545321666

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