ClinVar Miner

Submissions for variant NM_019851.3(FGF20):c.*182C>T

gnomAD frequency: 0.05484  dbSNP: rs12720208
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001723539 SCV001950753 benign not provided 2021-06-19 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 20427658, 18252210, 30241547)
OMIM RCV000005162 SCV000025339 uncertain significance Parkinson disease, late-onset 2009-02-15 no assertion criteria provided literature only

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