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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED12L, P2RY14
(P301L)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
TM4SF18, TM4SF4
+28 more
Deletion
Glycogen storage disease XV
+1 more
GPathogenic