ClinVar Miner

Submissions for variant NM_002965.4(S100A9):c.288G>A (p.Glu96=)

gnomAD frequency: 0.00001  dbSNP: rs752093810
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000937876 SCV001083670 likely benign not provided 2018-07-18 criteria provided, single submitter clinical testing

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