List of variants in gene combination PKD1, TSC2 reported as uncertain significance for Tuberous sclerosis 2

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000548.5(TSC2):c.5028G>A (p.Leu1676=)	rs45475501	0.00030
NC_000016.9:g.(?_2098588)_(2138713_?)dup
NC_000016.9:g.(?_2114273)_(2138713_?)dup
NC_000016.9:g.(?_2135221)_(2140114_?)dup

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