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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GLDN
(L20P)
Single nucleotide variant
(missense variant)
Lethal congenital contracture syndrome 11
GLikely pathogenic
GLDN
Single nucleotide variant
(splice donor variant)
Lethal congenital contracture syndrome 11
GUncertain significance