"Counsyl"[submitter] AND "LOC130061310"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 372087	NM_058216.3(RAD51C):c.145+2T>G	LOC130061310, RAD51C	Single nucleotide variant (splice donor variant)	Fanconi anemia complementation group O +2 more	GPathogenic/Likely pathogenic
Select item 138870	NM_058216.3(RAD51C):c.145+12T>G	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 3 +4 more	GConflicting classifications of pathogenicity