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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STX1A
(I182V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
LOC129998608, STX1A
(R9H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance