ClinVar Miner

Submissions for variant NM_004465.2(FGF10):c.626A>G (p.Ter209Trp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn RCV004776552 SCV005387927 likely pathogenic Interstitial lung disease specific to childhood 2024-09-23 criteria provided, single submitter clinical testing

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