List of variants reported as uncertain significance for Hereditary renal cell carcinoma

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_016292.3(TRAP1):c.1604C>G (p.Thr535Ser)	rs77440336	0.00838
NM_004168.4(SDHA):c.133G>A (p.Ala45Thr)	rs140736646	0.00060
NM_001963.6(EGF):c.47G>C (p.Ser16Thr)	rs200394315	0.00014
NM_001618.4(PARP1):c.370A>G (p.Thr124Ala)	rs139924814	0.00006

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