ClinVar Miner

List of variants in gene TSC1 reported as uncertain significance for bone benign neoplasm

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
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_000368.5(TSC1):c.1231C>A (p.Leu411Ile)	rs397514840	0.00003
NM_000368.5(TSC1):c.1355G>C (p.Gly452Ala)	rs371093730	0.00001

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