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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ELP6
(L118W +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely pathogenic
OTUD6B
(I143R +1 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies
GLikely pathogenic
OTUD6B
(V176fs +1 more)
Microsatellite
(frameshift variant)
Inborn genetic diseases
+1 more
GPathogenic/Likely pathogenic
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