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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AGPAT2
(W168*)
Single nucleotide variant
(nonsense +1 more)
Congenital generalized lipodystrophy type 1
GPathogenic
AGPAT2
Deletion
(splice donor variant)
Congenital generalized lipodystrophy type 1
GUncertain significance