C1860707[trait identifier] AND "Centogene AG - the Rare Disease Compan - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 49923	NM_000548.5(TSC2):c.848+281C>T	TSC2	Single nucleotide variant (intron variant)	Lymphangiomyomatosis +3 more	GPathogenic
Select item 486658	NM_000548.5(TSC2):c.1187A>T (p.Asp396Val)	TSC2 (D396V +4 more)	Single nucleotide variant (missense variant)	Tuberous sclerosis syndrome +2 more	GUncertain significance
Select item 207783	NM_000548.5(TSC2):c.2701C>T (p.Arg901Cys)	TSC2 (R901C +4 more)	Single nucleotide variant (missense variant)	Tuberous sclerosis 2 +2 more	GConflicting classifications of pathogenicity

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