List of variants in gene combination LOC130061310, RAD51C reported as uncertain significance for Hereditary cancer-predisposing syndrome

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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_058216.3(RAD51C):c.145+5C>A	rs876660577	0.00001
NM_058216.3(RAD51C):c.145+5C>T	rs876660577	0.00001
NM_058216.3(RAD51C):c.145+2_145+3insTT	rs1567783294
NM_058216.3(RAD51C):c.145+3A>G	rs536596205
NM_058216.3(RAD51C):c.145+5C>G
NM_058216.3(RAD51C):c.145+5_145+7delinsG	rs2047820619
NM_058216.3(RAD51C):c.145+6G>A

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