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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PIGL
(D113Y)
Single nucleotide variant
(missense variant)
CHIME syndrome
+1 more
GConflicting classifications of pathogenicity
PIGL
(L167P)
Single nucleotide variant
(missense variant)
Coloboma, Congenital Heart Disease, Ichthyosiform Dermatosis, Intellectual Disability, and Ear Anomalies (CHIME) Syndrome
+3 more
GPathogenic