ClinVar Miner

Submissions for variant NM_032531.4(KIRREL3):c.396C>T (p.Ala132=)

gnomAD frequency: 0.00065  dbSNP: rs35152573
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000193418 SCV000247747 uncertain significance not specified 2014-12-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000899522 SCV001043798 likely benign not provided 2018-12-10 criteria provided, single submitter clinical testing

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