List of variants in gene RAD50 reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005732.4(RAD50):c.2014C>T (p.Gln672Ter)	rs142947311	0.00002
NM_005732.4(RAD50):c.2821C>T (p.Gln941Ter)	rs397507177	0.00001
NM_005732.4(RAD50):c.3050G>A (p.Trp1017Ter)	rs1554099776	0.00001

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