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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TREM2
(V126G)
Single nucleotide variant
(missense variant)
TREM2-related condition
+1 more
GPathogenic/Likely pathogenic
TREM2
(W78*)
Single nucleotide variant
(nonsense)
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2
GLikely pathogenic
TREM2
(T66M)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
TREM2
(Y38C)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
TREM2
(Q33*)
Single nucleotide variant
(nonsense)
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2
+1 more
GPathogenic
TREM2
Deletion
(intron variant)
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
GPathogenic/Likely pathogenic
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