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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TSC2
Single nucleotide variant
(intron variant)
Tuberous sclerosis 2
GUncertain significance
TSC2
Single nucleotide variant
(splice donor variant)
Tuberous sclerosis 2
GPathogenic
TSC2
(L479fs +4 more)
Deletion
(frameshift variant)
Tuberous sclerosis 2
GPathogenic
PKD1, TSC2
(L3952P +1 more)
Single nucleotide variant
(missense variant)
Lymphangiomyomatosis
+2 more
GUncertain significance
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