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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBN1
(G1879D)
Single nucleotide variant
(missense variant)
Marfan syndrome
GPathogenic
FBN1
(G1571D)
Single nucleotide variant
(missense variant)
Progeroid and marfanoid aspect-lipodystrophy syndrome
GUncertain significance