ClinVar Miner

Submissions for variant NM_019842.4(KCNQ5):c.2164G>A (p.Asp722Asn)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002643580 SCV002982758 benign not provided 2022-06-13 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002643580 SCV004011683 uncertain significance not provided 2023-04-01 criteria provided, single submitter clinical testing

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