ClinVar Miner

Submissions for variant NM_015100.4(POGZ):c.2792C>T (p.Pro931Leu)

gnomAD frequency: 0.00011  dbSNP: rs373783340
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000754519 SCV000803231 association Autism spectrum disorder no assertion criteria provided clinical testing

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