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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPTBN1
Indel
(splice acceptor variant)
Intellectual disability
+1 more
GUncertain significance
LOC126862264, MEFV
Single nucleotide variant
(missense variant +1 more)
not provided
+24 more
GPathogenic/Likely pathogenic
TNRC6B
Single nucleotide variant
(intron variant +1 more)
Autistic behavior
+2 more
GUncertain significance
TNRC6B
(Q1212* +2 more)
Single nucleotide variant
(nonsense)
Autistic behavior
+2 more
GUncertain significance
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