ClinVar Miner

Submissions for variant NM_002246.3(KCNK3):c.615C>T (p.Tyr205=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005024386 SCV005655922 uncertain significance Pulmonary hypertension, primary, 4 2023-12-29 criteria provided, single submitter clinical testing

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