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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDR35
(L1024V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WDR35
Single nucleotide variant
(synonymous variant)
Short-rib thoracic dysplasia 7 with or without polydactyly
+2 more
GUncertain significance
WDR35
(S634Y +1 more)
Single nucleotide variant
(missense variant)
Short-rib thoracic dysplasia 7 with or without polydactyly
+2 more
GUncertain significance
WDR35
(L641* +1 more)
Single nucleotide variant
(nonsense)
WDR35-related disorder
+4 more
GPathogenic/Likely pathogenic
WDR35
(I515V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
WDR35
(N466fs +1 more)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
WDR35
(F406S)
Single nucleotide variant
(missense variant +1 more)
Short-rib thoracic dysplasia 7 with or without polydactyly
+2 more
GUncertain significance
WDR35
Single nucleotide variant
(splice donor variant)
not provided
GPathogenic
WDR35
(G146A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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