List of variants in gene RAD50 reported as benign by Ambry Genetics

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_005732.4(RAD50):c.2025C>T (p.Asp675=)	rs34147298	0.02660
NM_005732.4(RAD50):c.3037-3T>C	rs115737081	0.00627
NM_005732.4(RAD50):c.572C>T (p.Thr191Ile)	rs2230017	0.00469
NM_005732.4(RAD50):c.280A>C (p.Ile94Leu)	rs28903085	0.00300
NM_005732.4(RAD50):c.2670G>A (p.Gln890=)	rs112241748	0.00216
NM_005732.4(RAD50):c.980G>A (p.Arg327His)	rs28903091	0.00207
NM_005732.4(RAD50):c.2091C>T (p.Val697=)	rs61747588	0.00156
NM_005732.4(RAD50):c.379G>A (p.Val127Ile)	rs28903086	0.00146
NM_005732.4(RAD50):c.3165-4A>T	rs104895050	0.00133
NM_005732.4(RAD50):c.671G>A (p.Arg224His)	rs28903088	0.00065

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