List of variants in gene RAD51C reported as likely pathogenic by Quest Diagnostics Nichols Institute San Juan Capistrano

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.773G>A (p.Arg258His)	rs267606997	0.00002
NM_058216.3(RAD51C):c.904+5G>T	rs587782702	0.00001
NM_058216.3(RAD51C):c.404G>C (p.Cys135Ser)	rs767796996
NM_058216.3(RAD51C):c.904+1G>T	rs1555602159
NM_058216.3(RAD51C):c.994C>T (p.Gln332Ter)	rs1555605074

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