ClinVar Miner

Submissions for variant NM_017946.4(FKBP14):c.198-324T>C

gnomAD frequency: 0.00354  dbSNP: rs77077786
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001575377 SCV001802357 likely benign not provided 2018-08-25 criteria provided, single submitter clinical testing

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