Related gene-specific medical variations for Gene (Select 5888) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3360169	NM_002875.5(RAD51):c.322G>A (p.Glu108Lys)	RAD51 (E108K)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3067851	NM_002875.5(RAD51):c.225+633A>C	RAD51 (E85A)	Single nucleotide variant (missense variant +1 more)	Mirror movements 2	GUncertain significance
Select item 2445281	NM_002875.5(RAD51):c.225+719A>C	RAD51 (T114P)	Single nucleotide variant (missense variant +1 more)	Ovarian cancer	GBenign
Select item 2443994	NM_002875.5(RAD51):c.871ATC[1] (p.Ile292del)	RAD51 (I292del +1 more)	Microsatellite (inframe_deletion +1 more)	Fanconi anemia complementation group R	GLikely pathogenic
Select item 1243349	NM_002875.5(RAD51):c.-61G>T	LOC130056864, RAD51	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 13128	NM_002875.5(RAD51):c.-98G>C	LOC130056864, RAD51	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign

ClinVar