List of variants reported as likely benign for benign neoplasm by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002028.4(FNTB):c.209+1976G>T	rs201052112	0.00047
NM_133171.5(ELMO2):c.1416+9C>G	rs770529533	0.00002
NM_002382.5(MAX):c.172-6278_172-6277del

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