List of variants reported as likely pathogenic for breast carcinoma by MVZ Praenatalmedizin und Genetik Nuernberg

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.7089+1G>T	rs777741666
NM_000051.4(ATM):c.8054C>A (p.Ser2685Ter)	rs2086676230
NM_000051.4(ATM):c.9068del (p.Gly3023fs)	rs1591387383
NM_024675.4(PALB2):c.3446_3447insAGTACAGC (p.Leu1150fs)	rs2142253658

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