List of variants in gene combination BRCA2, LOC106721785 reported as likely benign for Hereditary breast ovarian cancer syndrome

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.-41G>A	rs879255312	0.00004
NM_000059.4(BRCA2):c.-40+11G>A	rs1321905463	0.00001
NM_000059.4(BRCA2):c.-40+7G>T	rs1555279969	0.00001
NM_000059.3(BRCA2):c.-220G>T	rs1036870835
NM_000059.4(BRCA2):c.-40+10G>A
NM_000059.4(BRCA2):c.-40+10G>T
NM_000059.4(BRCA2):c.-40+13G>A	rs1593879857
NM_000059.4(BRCA2):c.-40+14G>T	rs2138695788
NM_000059.4(BRCA2):c.-40+16A>G
NM_000059.4(BRCA2):c.-40+17G>A	rs2138695806
NM_000059.4(BRCA2):c.-40+20G>A	rs2138695820
NM_000059.4(BRCA2):c.-40+20G>T	rs2138695820
NM_000059.4(BRCA2):c.-40+3T>C	rs2138695729
NM_000059.4(BRCA2):c.-40+5GTG[4]	rs2072249252
NM_000059.4(BRCA2):c.-40+7G>A	rs1555279969
NM_000059.4(BRCA2):c.-40+8G>A	rs2138695764
NM_000059.4(BRCA2):c.-42C>A	rs536354307
NM_000059.4(BRCA2):c.-42C>G	rs536354307
NM_000059.4(BRCA2):c.-42_-41del	rs899298231
NM_000059.4(BRCA2):c.-45G>C	rs2138695684
NM_000059.4(BRCA2):c.-50C>A	rs2138695676
NM_000059.4(BRCA2):c.-55T>C	rs2138695628
NM_000059.4(BRCA2):c.-56_-55insCTC	rs2138695618
NM_000059.4(BRCA2):c.-56del	rs1593879808
NM_000059.4(BRCA2):c.-59_-57del	rs545321666

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