ClinVar Miner

List of variants in gene combination BRCA2, LOC106721785 reported as likely benign for not specified

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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.-41G>A rs879255312 0.00004
NM_000059.4(BRCA2):c.-42_-41del rs899298231
NM_000059.4(BRCA2):c.-50_-48del rs1555279965
NM_000059.4(BRCA2):c.-51C>T rs1057521841
NM_000059.4(BRCA2):c.-55_-52delinsCTCCGCG rs1555279959
NM_000059.4(BRCA2):c.-56C>A rs1555279958
NM_000059.4(BRCA2):c.-60A>G rs1057522793

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