List of variants in gene BRCA2 reported as likely pathogenic for Breast carcinoma

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)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.10095delinsGAATTATATCT (p.Ser3366fs)	rs276174803
NM_000059.4(BRCA2):c.1813dup (p.Ile605fs)	rs80359306
NM_000059.4(BRCA2):c.3451_3454del (p.Thr1150_Ile1151insTer)	rs2137496671
NM_000059.4(BRCA2):c.6841+2T>G	rs1593909960
NM_000059.4(BRCA2):c.8995_8996del (p.Leu2999fs)	rs2137622356

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