ClinVar Miner

List of variants reported as likely benign for Noonan syndrome with multiple lentigines by Illumina Laboratory Services, Illumina

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Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_002834.5(PTPN11):c.*1006del rs146940557 0.05739
NM_002880.3(RAF1):c.-415-1C>G rs61730434 0.01127
NM_002834.5(PTPN11):c.*1157ATG[14] rs80269561
NM_002880.4(RAF1):c.321-14dup rs202103447
NM_004333.6(BRAF):c.2128-5del rs373442098

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