ClinVar Miner

Submissions for variant NM_014907.3(FRMPD1):c.770G>A (p.Arg257His)

gnomAD frequency: 0.00335  dbSNP: rs148192224
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Oncology - Human Genetics Lab, University of Sao Paulo RCV001843910 SCV002103140 uncertain significance Hepatoblastoma no assertion criteria provided research

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