ClinVar Miner

List of variants in gene BRCA2 reported as likely pathogenic for not specified

Minimum submission review status:		Collection method:
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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 1

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HGVS	dbSNP
NM_000059.3(BRCA2):c.8755-1G>A	rs81002812

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