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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PAFAH1B3
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ACTMAP, AKT2
+84 more
Duplication
MEGF8-related Carpenter syndrome
+3 more
GUncertain significance