List of variants reported as uncertain significance for childhood malignant neoplasm by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_177438.3(DICER1):c.1377-18T>A	rs1032236740	0.00002
NM_177438.3(DICER1):c.920G>A (p.Arg307His)	rs149718671	0.00001
NM_177438.3(DICER1):c.2210C>T (p.Pro737Leu)	rs1595391071
NM_177438.3(DICER1):c.5171C>T (p.Pro1724Leu)	rs749900564

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