ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.4206+13G>T

gnomAD frequency: 0.00018  dbSNP: rs398043696
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003393585 SCV004130318 benign not provided 2022-10-01 criteria provided, single submitter clinical testing DICER1: BS1, BS2

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