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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LZTR1, LOC130067016
(Q10fs)
Deletion
(frameshift variant)
Noonan syndrome 10
+5 more
GPathogenic
LZTR1
(P701L)
Single nucleotide variant
(missense variant)
Noonan syndrome 2
GUncertain significance