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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129991989, MAEA
(M12V)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
LOC129991989, MAEA
(L22F)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance