List of variants reported as uncertain significance for bone benign neoplasm by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_015922.3(NSDHL):c.263G>A (p.Arg88Gln)	rs781879080	0.00002
NM_015922.3(NSDHL):c.560A>G (p.Asn187Ser)	rs782332983	0.00002
NM_015922.3(NSDHL):c.947C>G (p.Pro316Arg)	rs782141957	0.00002
NM_015922.3(NSDHL):c.265C>G (p.Gln89Glu)	rs145580873	0.00001
NM_015922.3(NSDHL):c.1031A>G (p.Lys344Arg)	rs2125017628
NM_015922.3(NSDHL):c.1054C>G (p.Leu352Val)	rs142351862

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