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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASCC3
(L1999P)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder, autosomal recessive 81
+1 more
GUncertain significance
ASCC3
Single nucleotide variant
(splice acceptor variant)
Intellectual developmental disorder, autosomal recessive 81
+1 more
GUncertain significance