ClinVar Miner

Submissions for variant NM_015937.6(PIGT):c.365+17G>T

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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 RCV003068312 SCV003450528 likely benign Multiple congenital anomalies-hypotonia-seizures syndrome 3 2022-09-02 criteria provided, single submitter clinical testing

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