List of variants reported as likely pathogenic for benign neoplasm by Solve-RD Consortium

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005343.4(HRAS):c.37G>T (p.Gly13Cys)	rs104894228
NM_005343.4(HRAS):c.38G>T (p.Gly13Val)	rs104894226
NM_006218.4(PIK3CA):c.263G>A (p.Arg88Gln)	rs121913287
NM_006218.4(PIK3CA):c.3140A>G (p.His1047Arg)	rs121913279

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