List of variants reported as pathogenic for acute lymphoblastic leukemia by OMIM

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.7271T>G (p.Val2424Gly)	rs28904921	0.00006
NM_002074.5(GNB1):c.239T>A (p.Ile80Asn)	rs752746786	0.00001
NM_000051.4(ATM):c.5044G>C (p.Asp1682His)	rs121434217
NM_000051.4(ATM):c.5309C>G (p.Ser1770Ter)	rs121434223
NM_000051.4(ATM):c.7638_7646del (p.Arg2547_Ser2549del)	rs587776547
NM_002074.5(GNB1):c.227A>G (p.Asp76Gly)	rs869312821
NM_002467.6(MYC):c.162G>C (p.Glu54Asp)	rs121918684
NM_002467.6(MYC):c.214C>T (p.Pro72Ser)	rs28933407
NM_002467.6(MYC):c.220C>G (p.Pro74Ala)	rs121918685
NM_002467.6(MYC):c.302A>C (p.Asn101Thr)	rs121918683
NM_003921.5(BCL10):c.136dup (p.Ile46fs)	rs387906351
NM_004119.3(FLT3):c.1777_1779del (p.Asp593del)	rs587776834
NM_004119.3(FLT3):c.2503G>T (p.Asp835Tyr)	rs121913488
NM_004119.3(FLT3):c.2504A>T (p.Asp835Val)	rs121909646
NM_016734.3(PAX5):c.239C>G (p.Pro80Arg)
NM_138761.4(BAX):c.115_121del (p.Gly39fs)	rs398122840
NM_138761.4(BAX):c.199G>A (p.Gly67Arg)	rs398122513

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