ClinVar Miner

List of variants in gene BRCA2 reported as likely pathogenic by Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine

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Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.6842-2A>G rs1555285132
NM_000059.4(BRCA2):c.7007G>T (p.Arg2336Leu) rs28897743
NM_000059.4(BRCA2):c.8168A>C (p.Asp2723Ala) rs41293513

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