ClinVar Miner

Submissions for variant NM_005027.4(PIK3R2):c.1808+16G>A

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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 RCV005177519 SCV005805265 likely benign Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1 2024-05-06 criteria provided, single submitter clinical testing

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