ClinVar Miner

Submissions for variant NM_015158.5(KANK1):c.52A>G (p.Ile18Val)

gnomAD frequency: 0.01415  dbSNP: rs61737970
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001768168 SCV002008610 likely benign not provided 2025-03-11 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Labcorp Genetics (formerly Invitae), Labcorp RCV001768168 SCV002453530 benign not provided 2025-01-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001768168 SCV005223040 likely benign not provided criteria provided, single submitter not provided

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