List of variants in gene RAD51C reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
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: 7

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.224dup (p.Tyr75Ter)	rs730881939	0.00002
NM_058216.3(RAD51C):c.706-2A>G	rs587780259	0.00002
NM_058216.3(RAD51C):c.905-2A>C	rs779582317	0.00001
NM_058216.3(RAD51C):c.905-2_905-1del	rs587781995	0.00001
NM_058216.3(RAD51C):c.905-2del	rs876658652	0.00001
NM_058216.3(RAD51C):c.409C>T (p.Gln137Ter)	rs2048021234
NM_058216.3(RAD51C):c.525dup (p.Cys176fs)	rs768793789

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