List of variants in gene RAD51C reported as benign for Fanconi anemia complementation group O

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.904+34T>C	rs28363318	0.30375
NM_058216.3(RAD51C):c.90G>A (p.Ala30=)	rs115414895	0.01193
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.837+13T>C	rs188613030	0.00112
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.1026+13T>C	rs531535812
NM_058216.3(RAD51C):c.1027-10del	rs768715761
NM_058216.3(RAD51C):c.1027-10dup	rs768715761
NM_058216.3(RAD51C):c.146-9del
NM_058216.3(RAD51C):c.459T>G (p.Gly153=)	rs769486350
NM_058216.3(RAD51C):c.572-11del	rs587780258

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