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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130006222, LOC130006223
+282 more
Copy number loss
See cases
GPathogenic
LOC130006108, LOC130006109
+72 more
Duplication
Cutis laxa, autosomal recessive, type 1B
GUncertain significance