List of variants reported as likely benign for bone benign neoplasm

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_015922.3(NSDHL):c.1054C>T (p.Leu352=)	rs142351862	0.00444
NM_015922.3(NSDHL):c.893G>T (p.Trp298Leu)	rs139186585	0.00143
NM_015922.3(NSDHL):c.306C>T (p.Phe102=)	rs141089248	0.00138
NM_015922.3(NSDHL):c.834C>T (p.Phe278=)	rs149698967	0.00057
NM_015922.3(NSDHL):c.351T>C (p.Phe117=)	rs138711934	0.00045
NM_015922.3(NSDHL):c.678C>T (p.Phe226=)	rs147293409	0.00044
NM_015922.3(NSDHL):c.987C>T (p.Val329=)	rs149122192	0.00017
NM_015922.3(NSDHL):c.612C>T (p.Phe204=)	rs782252634	0.00001
NM_015922.3(NSDHL):c.268-15dup	rs782031217
NM_015922.3(NSDHL):c.796C>T (p.His266Tyr)

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