List of variants reported as likely benign for small intestine neoplasm by Fulgent Genetics, Fulgent Genetics

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.8C>G (p.Ala3Gly)	rs11203289	0.01309
NM_003000.3(SDHB):c.32G>A (p.Arg11His)	rs111430410	0.00185
NM_003000.3(SDHB):c.300T>C (p.Ser100=)	rs11541235	0.00157
NM_000222.3(KIT):c.2502G>A (p.Lys834=)	rs146992614	0.00014
NM_003001.5(SDHC):c.405+13G>A	rs369274171	0.00008
NM_000222.3(KIT):c.840G>C (p.Ala280=)	rs142772432	0.00004
NM_000222.3(KIT):c.531C>T (p.Arg177=)	rs756722358	0.00001
NM_003000.3(SDHB):c.424-37TTC[10]	rs34261028

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