ClinVar Miner

Submissions for variant NM_002246.3(KCNK3):c.774C>T (p.Ala258=)

dbSNP: rs1243931857
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001463029 SCV001666959 likely benign Pulmonary hypertension, primary, 4 2018-09-28 criteria provided, single submitter clinical testing

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