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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TPH2
(R237Q)
Single nucleotide variant
(missense variant)
Major depressive disorder
+1 more
GUncertain significance
TPH2
(S41Y)
Single nucleotide variant
(missense variant)
Tryptophan 5-monooxygenase deficiency
+3 more
GLikely benign
APOE
(L151M +1 more)
Single nucleotide variant
(missense variant)
Major depressive disorder
Gnot provided
APOE
(L122M +1 more)
Single nucleotide variant
(missense variant)
Major depressive disorder
Gnot provided
TPH2
(P206S)
Single nucleotide variant
(missense variant)
Tryptophan 5-monooxygenase deficiency
+2 more
GUncertain significance
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