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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TREM2
(S116C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TREM2
(N68I)
Single nucleotide variant
(missense variant)
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2
GUncertain significance