ClinVar Miner

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

Included ClinVar conditions (17):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.397C>T (p.Arg133Ter)	rs764575966	0.00001
NM_003000.3(SDHB):c.166_170del (p.Pro56fs)	rs786202100

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