ClinVar Miner

Submissions for variant NM_001368397.1(FRMPD4):c.981T>C (p.Tyr327=)

gnomAD frequency: 0.00002  dbSNP: rs779013797
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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 for Human Genetics, Inc, Center for Human Genetics, Inc RCV000659680 SCV000781525 likely benign Autism, susceptibility to, X-linked 4 2016-11-01 criteria provided, single submitter clinical testing

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