ClinVar Miner

List of variants in gene PTPN11 reported as likely benign for History of neurodevelopmental disorder

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Total variants: 6
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HGVS dbSNP
NM_002834.4(PTPN11):c.1551G>A (p.Ala517=) rs727504377
NM_002834.4(PTPN11):c.1650G>A (p.Ala550=) rs374896287
NM_002834.4(PTPN11):c.1658C>T (p.Thr553Met) rs148176616
NM_002834.4(PTPN11):c.438T>C (p.Asp146=) rs1566168661
NM_002834.4(PTPN11):c.558G>T (p.Arg186=) rs200920312
NM_002834.4(PTPN11):c.951G>A (p.Lys317=) rs576405446

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