ClinVar Miner

Submissions for variant NM_033310.3(KCNK4):c.475-5C>T

gnomAD frequency: 0.00002  dbSNP: rs200735754
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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 RCV002085354 SCV002371202 likely benign not provided 2021-11-17 criteria provided, single submitter clinical testing

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