List of variants in gene combination RAD50, TH2LCRR reported as benign for Hereditary cancer-predisposing syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005732.4(RAD50):c.3846T>C (p.Tyr1282=)	rs1804670	0.05209
NM_005732.4(RAD50):c.3879C>T (p.Ile1293=)	rs28903094	0.00293
NM_005732.4(RAD50):c.3790C>T (p.Leu1264Phe)	rs199579239	0.00009
NM_005732.4(RAD50):c.3902A>G (p.Lys1301Arg)	rs201766077	0.00001

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