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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NTRK2
Single nucleotide variant
(intron variant)
Developmental and epileptic encephalopathy, 58
+2 more
GBenign/Likely benign
NTRK2
(S11Y +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+5 more
GLikely benign
NTRK2
Deletion
(intron variant)
Developmental and epileptic encephalopathy, 58
+2 more
GBenign/Likely benign
NTRK2
(V361I +4 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
NTRK2
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GLikely benign
NTRK2
Single nucleotide variant
(synonymous variant)
NTRK2-related disorder
+4 more
GBenign/Likely benign
NTRK2
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign/Likely benign
NTRK2
Single nucleotide variant
(synonymous variant)
Developmental and epileptic encephalopathy, 58
+3 more
GLikely benign
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