ClinVar Miner

Submissions for variant NM_001377458.1(CLCC1):c.1180G>A (p.Gly394Ser)

dbSNP: rs745516722
Minimum review status: Collection method:
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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 RCV001317822 SCV001508499 uncertain significance not provided 2021-09-01 criteria provided, single submitter clinical testing

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