ClinVar Miner

List of variants in gene TSC2 reported as uncertain significance by Institute of Human Genetics, University Hospital Muenster

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000548.5(TSC2):c.5116C>T (p.Arg1706Cys)	rs45517391	0.00029
NM_000548.5(TSC2):c.429C>G (p.Phe143Leu)	rs137854406	0.00003

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