List of variants reported as pathogenic for benign neoplasm by Clinical Genomics Laboratory, Washington University in St. Louis

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.35G>A (p.Gly12Asp)	rs121913529	0.00001
NM_000142.5(FGFR3):c.742C>T (p.Arg248Cys)	rs121913482
NM_002067.5(GNA11):c.627G>T (p.Gln209His)
NM_002524.5(NRAS):c.182A>G (p.Gln61Arg)	rs11554290
NM_004985.5(KRAS):c.35G>T (p.Gly12Val)	rs121913529
NM_005343.4(HRAS):c.34G>A (p.Gly12Ser)	rs104894229

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