List of variants in gene combination BRCA2, LOC106721785 studied for Hereditary cancer-predisposing syndrome

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.-175C>T	rs55880202	0.00642
NM_000059.4(BRCA2):c.-296C>T	rs563971900	0.00228
NM_000059.4(BRCA2):c.-40+7G>T	rs1555279969	0.00001
NM_000059.4(BRCA2):c.-88G>T	rs917232759	0.00001
NM_000059.3(BRCA2):c.-220G>T	rs1036870835
NM_000059.4(BRCA2):c.-188C>T	rs556172218
NM_000059.4(BRCA2):c.-40+1G>A	rs2072249096
NM_000059.4(BRCA2):c.-40+2T>C	rs1593879845
NM_000059.4(BRCA2):c.-40+7G>A	rs1555279969
NM_000059.4(BRCA2):c.-40G>C	rs1555279967
NM_000059.4(BRCA2):c.-40G>T	rs1555279967

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