ClinVar Miner

Submissions for variant NM_015100.4(POGZ):c.1940A>C (p.Tyr647Ser)

dbSNP: rs749548928
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center of Medical Genetics, Central South University RCV000754528 SCV000803240 association Autism spectrum disorder no assertion criteria provided clinical testing

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