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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RRAS2
(Q37L +1 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
Noonan syndrome
GPathogenic
LOC130005368, RRAS2
Duplication
(inframe_insertion +1 more)
Noonan syndrome 12
+3 more
GPathogenic