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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ECEL1
(L165P)
Single nucleotide variant
(missense variant)
Arthrogryposis multiplex congenita
+3 more
GConflicting classifications of pathogenicity
ECEL1
(P34S)
Single nucleotide variant
(missense variant)
Distal arthrogryposis type 5D
+1 more
GUncertain significance