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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TREM2
(D216Y)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
TREM2
(R62C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TREM2
(Y38*)
Single nucleotide variant
(nonsense)
not provided
GLikely pathogenic
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