List of variants in gene RAD50 reported as likely benign by GeneDx

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_005732.4(RAD50):c.2207+296G>A	rs115976537	0.01975
NM_005732.4(RAD50):c.1970-65G>A	rs148383531	0.01409
NM_005732.4(RAD50):c.130-265A>G	rs115198557	0.00903
NM_005732.4(RAD50):c.1794-193A>C	rs73259670	0.00440
NM_005732.4(RAD50):c.757-63C>T	rs74861356	0.00403
NM_005732.4(RAD50):c.213+203T>C	rs77099043	0.00372
NM_005732.4(RAD50):c.3164+49G>C	rs143829407	0.00361
NM_005732.4(RAD50):c.3036+151C>T	rs546261138	0.00308
NM_005732.4(RAD50):c.280A>C (p.Ile94Leu)	rs28903085	0.00300
NM_005732.4(RAD50):c.129+184T>G	rs2548986
NM_005732.4(RAD50):c.1969+232G>A	rs143331722
NM_005732.4(RAD50):c.2207+203dup	rs34713748
NM_005732.4(RAD50):c.2524+236del	rs879833449

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