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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HNRNPA3
(D13A)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
HNRNPA3
(G278A +1 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance