ClinVar Miner

Submissions for variant NM_000899.5(KITLG):c.67G>A (p.Val23Ile)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV003229223 SCV003925947 uncertain significance not provided 2022-11-21 criteria provided, single submitter clinical testing In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Labcorp Genetics (formerly Invitae), Labcorp RCV003229223 SCV004655420 benign not provided 2023-11-18 criteria provided, single submitter clinical testing

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