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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHST3
(R357Q)
Single nucleotide variant
(missense variant)
not provided
+5 more
GBenign
CHST3
Single nucleotide variant
(synonymous variant)
Larsen syndrome
+3 more
GConflicting classifications of pathogenicity
CHST3
Single nucleotide variant
(synonymous variant)
Spondyloepiphyseal dysplasia with congenital joint dislocations
+3 more
GConflicting classifications of pathogenicity
CHST3
(L455V)
Single nucleotide variant
(missense variant)
Spondyloepiphyseal dysplasia with congenital joint dislocations
GLikely benign
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