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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TTC21B
(I1208V)
Single nucleotide variant
(missense variant)
Jeune thoracic dystrophy
+1 more
GUncertain significance
TTC21B
(L592S)
Single nucleotide variant
(missense variant)
Nephrotic syndrome
GUncertain significance
TTC21B, TTC21B-AS1
(L223V)
Single nucleotide variant
(missense variant)
Jeune thoracic dystrophy
+1 more
GUncertain significance
TTC21B-AS1, TTC21B
(P209L)
Single nucleotide variant
(missense variant)
Asphyxiating thoracic dystrophy 4
+7 more
GPathogenic/Likely pathogenic
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