List of variants reported as likely pathogenic for Breast neoplasm

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.1427C>T (p.Thr476Met)	rs142763740	0.00032
NM_000059.4(BRCA2):c.8632G>A (p.Glu2878Lys)	rs398122710
NM_000546.6(TP53):c.526T>C (p.Cys176Arg)	rs967461896
NM_007194.4(CHEK2):c.1504del (p.Glu502fs)	rs1601702086
NM_007294.4(BRCA1):c.192T>G (p.Cys64Trp)	rs587781632
NM_007294.4(BRCA1):c.5141T>G (p.Val1714Gly)	rs80357243

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