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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC122056894, NFIA
(C4Y)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
LOC122056894, NFIA
(P32L)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance