ClinVar Miner

Submissions for variant NM_000036.2(AMPD1):c.826G>A (p.Asp276Asn) (rs587779379)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
State Key Lab of Medical Genetics, Central South University RCV000143856 SCV000109587 uncertain significance Autistic disorder of childhood onset criteria provided, single submitter reference population

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