Variants in gene RAD51C with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.428A>G (p.Gln143Arg)	rs587780255	0.00006
NM_058216.3(RAD51C):c.571+5G>A	rs145779113	0.00002
NM_058216.3(RAD51C):c.571+4A>G	rs587780257	0.00001
NM_058216.3(RAD51C):c.905-2_905-1del	rs587781995	0.00001
NM_058216.3(RAD51C):c.934C>T (p.Arg312Trp)	rs730881932	0.00001
NM_058216.3(RAD51C):c.935G>A (p.Arg312Gln)	rs779834376	0.00001
NM_058216.3(RAD51C):c.485G>A (p.Gly162Glu)	rs35151472
NM_058216.3(RAD51C):c.837+4_837+7del	rs727503760
NM_058216.3(RAD51C):c.904G>A (p.Gly302Arg)	rs1555602158

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