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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARL13B
(V22G)
Single nucleotide variant
(missense variant +3 more)
Joubert syndrome 8
GPathogenic
ARL13B
(W82* +1 more)
Single nucleotide variant
(nonsense +2 more)
Joubert syndrome 8
GPathogenic
ARL13B
(N154S +3 more)
Single nucleotide variant
(missense variant +1 more)
Joubert syndrome 8
+1 more
GConflicting classifications of pathogenicity
ARL13B
(R200C +3 more)
Single nucleotide variant
(missense variant +1 more)
Joubert syndrome and related disorders
+1 more
GPathogenic/Likely pathogenic
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