List of variants reported as uncertain significance for Hereditary cancer-predisposing syndrome by Center of Medical Genetics and Primary Health Care

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.1174C>A (p.Leu392Met)	rs144079536	0.00041
NM_000051.4(ATM):c.3371A>T (p.Tyr1124Phe)	rs876660498	0.00002
NM_001143992.2(WRAP53):c.1564del (p.Ala522fs)	rs755116516
NM_001184.4(ATR):c.1602G>C (p.Trp534Cys)	rs1577697163
NM_005431.2(XRCC2):c.268C>T (p.Leu90Phe)	rs587780127
NM_032444.4(SLX4):c.2320G>T (p.Ala774Ser)	rs1268731319

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