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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130010172, LOC130010173
+367 more
Copy number gain
See cases
GPathogenic
CHAMP1, LINC01054
(R497*)
Single nucleotide variant
(nonsense)
Inborn genetic diseases
+2 more
GPathogenic