ClinVar Miner

Submissions for variant NM_001136191.3(KANK2):c.1418-6C>T

gnomAD frequency: 0.01556  dbSNP: rs114414326
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000957919 SCV001104740 benign not provided 2024-01-28 criteria provided, single submitter clinical testing
GeneDx RCV000957919 SCV002013180 likely benign not provided 2021-04-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000957919 SCV005209402 likely benign not provided criteria provided, single submitter not provided

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