List of variants in gene TSC2 reported as uncertain significance by Mendelics

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000548.5(TSC2):c.538C>G (p.Leu180Val)	rs45485591	0.00003
NM_000548.5(TSC2):c.4550C>G (p.Pro1517Arg)	rs1279603512
NM_000548.5(TSC2):c.4876C>A (p.Pro1626Thr)	rs2090852831
NM_000548.5(TSC2):c.4936G>C (p.Val1646Leu)	rs1064796970
NM_000548.5(TSC2):c.5167T>C (p.Ser1723Pro)	rs45517408

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