ClinVar Miner

Submissions for variant NM_032242.4(PLXNA1):c.5030A>G (p.Glu1677Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005031091 SCV005659410 uncertain significance Dworschak-Punetha neurodevelopmental syndrome 2024-02-28 criteria provided, single submitter clinical testing

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