List of variants reported as likely pathogenic for small intestine neoplasm by “Giorgio Prodi” Cancer Research Center, University of Bologna

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.1741G>A (p.Gly581Arg)	rs771111180	0.00003
NM_004168.4(SDHA):c.1765C>T (p.Arg589Trp)	rs387906780	0.00002
NM_004168.4(SDHA):c.1766G>A (p.Arg589Gln)	rs763766162

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