List of variants in gene RAD51C reported as benign for not provided

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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_058216.3(RAD51C):c.904+34T>C	rs28363318	0.30375
NM_058216.3(RAD51C):c.838-319del	rs34147850	0.23564
NC_000017.11:g.58692526G>A	rs16943176	0.18609
NM_058216.3(RAD51C):c.-26C>T	rs12946397	0.18608
NM_058216.3(RAD51C):c.405-220T>C	rs9916423	0.14278
NM_058216.3(RAD51C):c.572-98C>G	rs6503874	0.14185
NM_058216.3(RAD51C):c.90G>A (p.Ala30=)	rs115414895	0.01193
NM_058216.3(RAD51C):c.405-49C>T	rs116809738	0.00838
NM_058216.3(RAD51C):c.859A>G (p.Thr287Ala)	rs28363317	0.00653
NM_058216.3(RAD51C):c.572-17G>T	rs193023469	0.00513
NM_058216.3(RAD51C):c.376G>A (p.Ala126Thr)	rs61758784	0.00349
NM_058216.3(RAD51C):c.186A>G (p.Gln62=)	rs28363303	0.00322
NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser)	rs147241704	0.00207
NM_058216.3(RAD51C):c.195A>G (p.Arg65=)	rs45511291	0.00105
NM_058216.3(RAD51C):c.146-8A>G	rs201079501	0.00074
NM_058216.3(RAD51C):c.706-18T>C	rs56401264	0.00047
NM_058216.3(RAD51C):c.*25C>G	rs28363336	0.00011
NM_058216.3(RAD51C):c.506T>C (p.Val169Ala)	rs587780256	0.00009
NM_058216.3(RAD51C):c.336G>A (p.Gly112=)	rs746122031	0.00006
NM_058216.3(RAD51C):c.870T>A (p.Ile290=)	rs376402418	0.00006
NM_058216.3(RAD51C):c.905-19T>C	rs368114768	0.00003
NM_058216.3(RAD51C):c.-13A>G	rs759669075	0.00002
NM_058216.3(RAD51C):c.-41T>C	rs373116323
NM_058216.3(RAD51C):c.572-16T>C	rs1555597053
NM_058216.3(RAD51C):c.837+351dup	rs71143280

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