List of variants in gene RAD51C reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 19

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HGVS	dbSNP	gnomAD frequency
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.790G>A (p.Gly264Ser)	rs147241704	0.00207
NM_058216.3(RAD51C):c.571+16A>G	rs141621051	0.00034
NM_058216.3(RAD51C):c.258A>T (p.Thr86=)	rs149228565	0.00017
NM_058216.3(RAD51C):c.744T>C (p.Phe248=)	rs150142859	0.00016
NM_058216.3(RAD51C):c.336G>A (p.Gly112=)	rs746122031	0.00006
NM_058216.3(RAD51C):c.813C>T (p.Ser271=)	rs376853755	0.00006
NM_058216.3(RAD51C):c.1062A>G (p.Ala354=)	rs201000407	0.00004
NM_058216.3(RAD51C):c.783A>G (p.Leu261=)	rs138643096	0.00003
NM_058216.3(RAD51C):c.-13A>G	rs759669075	0.00002
NM_058216.3(RAD51C):c.315A>G (p.Ser105=)	rs876660032	0.00002
NM_058216.3(RAD51C):c.453G>A (p.Val151=)	rs45553636	0.00002
NM_058216.3(RAD51C):c.513C>T (p.Asp171=)	rs140279158	0.00002
NM_058216.3(RAD51C):c.240G>A (p.Glu80=)	rs779053608	0.00001
NM_058216.3(RAD51C):c.-8A>G	rs768182004
NM_058216.3(RAD51C):c.572-11del	rs587780258
NM_058216.3(RAD51C):c.706-57TTA[3]	rs886038710
NM_058216.3(RAD51C):c.87T>C (p.Ser29=)	rs786203249

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