List of variants in gene BRCA2 reported as likely benign for Fanconi anemia complementation group A

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.6220C>A (p.His2074Asn)	rs34309943	0.00264
NM_000059.4(BRCA2):c.7626G>A (p.Thr2542=)	rs61754138	0.00228
NM_000059.4(BRCA2):c.1798T>C (p.Tyr600His)	rs75419644	0.00170
NM_000059.4(BRCA2):c.1938C>T (p.Ser646=)	rs28897711	0.00096
NM_000059.4(BRCA2):c.6921A>G (p.Ser2307=)	rs181183366	0.00019
NM_000059.4(BRCA2):c.3445A>G (p.Met1149Val)	rs80358589	0.00013
NM_000059.4(BRCA2):c.1909+9_1909+10del	rs527732001

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