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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129930471, POMGNT1
Deletion
(intron variant)
POMGNT1-related disorder
GLikely benign
LOC129930471, POMGNT1
Duplication
(intron variant)
POMGNT1-related disorder
GLikely benign