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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OFD1
(R639K +2 more)
Single nucleotide variant
(missense variant)
Simpson-Golabi-Behmel syndrome type 2
+4 more
GUncertain significance
OFD1
(E683del +2 more)
Microsatellite
(inframe_deletion)
Familial aplasia of the vermis
+2 more
GUncertain significance