List of variants in gene BRCA2 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.68-7T>A	rs81002830	0.00277
NM_000059.4(BRCA2):c.7150C>A (p.Gln2384Lys)	rs55977008	0.00203
NM_000059.4(BRCA2):c.8503T>C (p.Ser2835Pro)	rs11571746	0.00202
NM_000059.4(BRCA2):c.231T>G (p.Thr77=)	rs114446594	0.00191
NM_000059.4(BRCA2):c.1792A>G (p.Thr598Ala)	rs28897710	0.00182
NM_000059.4(BRCA2):c.4187A>G (p.Gln1396Arg)	rs55969723	0.00168
NM_000059.4(BRCA2):c.2803G>A (p.Asp935Asn)	rs28897716	0.00054
NM_000059.4(BRCA2):c.2350A>G (p.Met784Val)	rs11571653	0.00018
NM_000059.4(BRCA2):c.3055C>G (p.Leu1019Val)	rs55638633	0.00012
NM_000059.4(BRCA2):c.10045A>G (p.Thr3349Ala)	rs80358387	0.00010
NM_000059.4(BRCA2):c.4656T>C (p.Gly1552=)	rs41293491	0.00009
NM_000059.4(BRCA2):c.964A>C (p.Lys322Gln)	rs11571640	0.00001

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