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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PIGL
(D52fs)
Deletion
(frameshift variant)
CHIME syndrome
GLikely pathogenic
PIGL
(R88G)
Single nucleotide variant
(missense variant)
CHIME syndrome
GUncertain significance
PIGL
(L167P)
Single nucleotide variant
(missense variant)
Coloboma, Congenital Heart Disease, Ichthyosiform Dermatosis, Intellectual Disability, and Ear Anomalies (CHIME) Syndrome
+3 more
GPathogenic
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