List of variants in gene RAD50 reported as likely pathogenic by Sema4, Sema4

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005732.4(RAD50):c.1794-1G>A	rs587781742	0.00001
NM_005732.4(RAD50):c.552-1G>A	rs1236278956	0.00001
NM_005732.4(RAD50):c.1208_1209dup (p.Gln404fs)	rs786203655
NM_005732.4(RAD50):c.2095_2113dup (p.Leu705delinsGlnTer)	rs1750779319
NM_005732.4(RAD50):c.2202del (p.Pro734_Met735insTer)	rs786201789
NM_005732.4(RAD50):c.552-2A>C	rs1060501970

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