ClinVar Miner

Submissions for variant NM_001136191.3(KANK2):c.1194C>T (p.Asn398=)

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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 RCV003073234 SCV003477686 likely benign not provided 2023-01-03 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003073234 SCV004137810 likely benign not provided 2022-09-01 criteria provided, single submitter clinical testing KANK2: BP4, BP7

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