ClinVar Miner

Submissions for variant NM_152309.3(PIK3AP1):c.2352C>T (p.Ala784=)

dbSNP: rs1390796047
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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 RCV001401054 SCV001602869 likely benign Infantile spasms 2023-12-01 criteria provided, single submitter clinical testing

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