ClinVar Miner

Submissions for variant NM_001127178.3(PIGG):c.760-15T>C

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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 RCV003593072 SCV004282397 likely benign Intellectual disability, autosomal recessive 53 2024-05-15 criteria provided, single submitter clinical testing

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