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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAP2K2
(D221N)
Single nucleotide variant
(missense variant)
Cardiofaciocutaneous syndrome 4
+1 more
GUncertain significance
MAP2K2
(K172E)
Single nucleotide variant
(missense variant)
MAP2K2-related disorder
+10 more
GUncertain significance