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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMARCB1
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
SMARCB1
Single nucleotide variant
(intron variant)
not provided
GConflicting classifications of pathogenicity
SMARCB1
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GConflicting classifications of pathogenicity
SMARCB1
(H171R +3 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
SMARCB1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
SMARCB1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
SMARCB1
(K296N +3 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
SMARCB1
(D345Y +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCB1
Single nucleotide variant
(synonymous variant)
SMARCB1-related condition
+4 more
GBenign/Likely benign
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