List of variants in gene RAD51C reported as likely pathogenic for cancer

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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.706-2A>G	rs587780259	0.00002
NM_058216.3(RAD51C):c.1097G>A (p.Arg366Gln)	rs577852020	0.00001
NM_058216.3(RAD51C):c.1026+1G>C	rs1567817516
NM_058216.3(RAD51C):c.1026+5_1026+7del	rs587781410
NM_058216.3(RAD51C):c.394A>C (p.Thr132Pro)	rs2047959481
NM_058216.3(RAD51C):c.403T>C (p.Cys135Arg)	rs878855178
NM_058216.3(RAD51C):c.907G>A (p.Glu303Lys)

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