ClinVar Miner

List of variants reported as likely benign for not provided by Laboratory of Molecular Genetics (Pr. Bezieau's lab), CHU de Nantes

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Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_001039591.3(USP9X):c.5272G>A (p.Val1758Ile) rs2063195819
NM_001348800.3(ZBTB20):c.1099G>C (p.Glu367Gln) rs1560114223
NM_001493.3(GDI1):c.1237A>G (p.Thr413Ala) rs1569553475
NM_001614.5(ACTG1):c.526C>G (p.Leu176Val) rs782088589
NM_003072.5(SMARCA4):c.2247G>A (p.Met749Ile) rs2088721594
NM_004519.4(KCNQ3):c.994A>T (p.Ile332Phe) rs1563787859
NM_014795.4(ZEB2):c.659A>G (p.Tyr220Cys) rs1560609238
NM_015559.3(SETBP1):c.3434G>A (p.Gly1145Asp) rs1555707417

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