ClinVar Miner

List of variants reported as likely pathogenic for History of neurodevelopmental disorder by Ambry Genetics

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000489.6(ATRX):c.6149T>C (p.Ile2050Thr)	rs122445110
NM_002578.5(PAK3):c.276+5G>A	rs1569398792

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