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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNXB
(R3211G +1 more)
Single nucleotide variant
(missense variant)
Ehlers-Danlos syndrome due to tenascin-X deficiency
+4 more
GConflicting classifications of pathogenicity
TNXB
(V2919M +1 more)
Single nucleotide variant
(missense variant)
Vesicoureteral reflux 8
+4 more
GConflicting classifications of pathogenicity
TNXB
(I1934L)
Single nucleotide variant
(missense variant)
Vesicoureteral reflux 8
GUncertain significance
TNXB
(D677G)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
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