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Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TREM2
(W191*)
Single nucleotide variant
(nonsense +1 more)
not provided
+2 more
GBenign/Likely benign
TREM2
Single nucleotide variant
(intron variant)
not provided
GConflicting classifications of pathogenicity
TREM2
(L211P)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GBenign/Likely benign
TREM2
(H157Y)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
TREM2
(P144R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TREM2
(R136Q)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
TREM2
Single nucleotide variant
(synonymous variant)
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2
+3 more
GConflicting classifications of pathogenicity
TREM2
(A105V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TREM2
(R98W)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TREM2
(T96K)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
TREM2
(D87N)
Single nucleotide variant
(missense variant)
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2
+2 more
GConflicting classifications of pathogenicity
TREM2
(N68K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TREM2
(R62H)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
TREM2
(G58D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TREM2
(R47H)
Single nucleotide variant
(missense variant)
not specified
+3 more
GLikely benign
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