ClinVar Miner

Submissions for variant NM_002246.3(KCNK3):c.690G>A (p.Thr230=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005024387 SCV005655924 uncertain significance Pulmonary hypertension, primary, 4 2024-02-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005024387 SCV005777743 likely benign Pulmonary hypertension, primary, 4 2024-07-30 criteria provided, single submitter clinical testing

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