ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.2201_2202dup (p.Glu735fs)

dbSNP: rs762570903
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cancer Genomics Group, Japanese Foundation For Cancer Research RCV001030475 SCV001193583 likely pathogenic Hereditary breast ovarian cancer syndrome 2019-05-01 criteria provided, single submitter research

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