List of variants in gene combination RAD50, TH2-LCR, TH2LCRR reported as uncertain significance for carcinoma

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.3420G>A (p.Met1140Ile)	rs748377319	0.00004
NM_005732.4(RAD50):c.3539G>A (p.Arg1180Gln)	rs369788398	0.00001
NM_005732.4(RAD50):c.3488T>C (p.Ile1163Thr)	rs759753449

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