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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AGO2
(E787K +1 more)
Single nucleotide variant
(missense variant)
Lessel-Kreienkamp syndrome
GUncertain significance
AGO2
(D597H)
Single nucleotide variant
(missense variant)
Lessel-Kreienkamp syndrome
GUncertain significance
AGO2
(V93M)
Single nucleotide variant
(missense variant)
Lessel-Kreienkamp syndrome
GUncertain significance
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