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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WT1
Single nucleotide variant
(synonymous variant +1 more)
Nephroblastoma
+6 more
GConflicting classifications of pathogenicity
WT1
Single nucleotide variant
(synonymous variant +2 more)
Wilms tumor 1
+8 more
GBenign
WT1
Single nucleotide variant
(intron variant)
Frasier syndrome
+10 more
GBenign/Likely benign
WT1
Single nucleotide variant
(synonymous variant +2 more)
Nephroblastoma
+9 more
GBenign
WT1
(P37S +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+11 more
GConflicting classifications of pathogenicity
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+9 more
GBenign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
not specified
+8 more
GBenign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Nephrotic syndrome, type 4
+8 more
GBenign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Meacham syndrome
+9 more
GBenign/Likely benign
WT1, LOC107982234
Single nucleotide variant
(synonymous variant +1 more)
Wilms tumor 1
+9 more
GBenign/Likely benign
SMAD4
(P292L)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
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