ClinVar Miner

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

Included ClinVar conditions (69):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
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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