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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMARCA4
Single nucleotide variant
(synonymous variant +1 more)
Intellectual disability, autosomal dominant 16
+2 more
GConflicting classifications of pathogenicity
SMARCA4
(R1419C)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 16
+3 more
GConflicting classifications of pathogenicity
SMARCA4
Single nucleotide variant
(synonymous variant +1 more)
Rhabdoid tumor predisposition syndrome 2
+3 more
GConflicting classifications of pathogenicity
SMARCA4
(K1626R +5 more)
Single nucleotide variant
(missense variant +1 more)
Rhabdoid tumor predisposition syndrome 2
GUncertain significance
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