ClinVar Miner

Submissions for variant NM_001206999.2(CIT):c.5832C>T (p.Leu1944=)

gnomAD frequency: 0.00011  dbSNP: rs566427265
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000927303 SCV001072885 benign not provided 2018-10-23 criteria provided, single submitter clinical testing

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