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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMARCA4
Single nucleotide variant
(synonymous variant +1 more)
Coffin-Siris syndrome
+5 more
GBenign/Likely benign
SMARCA4
Single nucleotide variant
(synonymous variant +1 more)
not provided
+4 more
GConflicting classifications of pathogenicity
SMARCA4
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+4 more
GBenign/Likely benign
SMARCA4
Single nucleotide variant
(synonymous variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
SMARCA4
Single nucleotide variant
(3 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GBenign
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