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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMARCA4
(P244L)
Single nucleotide variant
(missense variant +1 more)
Rhabdoid tumor predisposition syndrome 2
+3 more
GConflicting classifications of pathogenicity
SMARCA4
Single nucleotide variant
(intron variant)
Intellectual disability, autosomal dominant 16
GUncertain significance
SMARCA4
(A1186V)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
SMARCA4
(E1610Q +5 more)
Single nucleotide variant
(missense variant +1 more)
Rhabdoid tumor predisposition syndrome 2
+1 more
GUncertain significance
SMARCA4
(V1658M +5 more)
Single nucleotide variant
(missense variant +1 more)
Rhabdoid tumor predisposition syndrome 2
+2 more
GConflicting classifications of pathogenicity
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