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Items: 16

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WT1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+8 more
GConflicting classifications of pathogenicity
WT1
(R250W +9 more)
Single nucleotide variant
(missense variant +1 more)
Mesothelioma, malignant
+9 more
GPathogenic/Likely pathogenic
WT1
Single nucleotide variant
(synonymous variant +2 more)
Frasier syndrome
+3 more
GLikely benign
WT1
Single nucleotide variant
(synonymous variant +2 more)
Frasier syndrome
+8 more
GBenign
WT1
Single nucleotide variant
(intron variant)
Nephrotic syndrome, type 4
+10 more
GBenign/Likely benign
WT1
Single nucleotide variant
(synonymous variant +2 more)
Nephroblastoma
+9 more
GBenign
WT1
Single nucleotide variant
(intron variant)
Wilms tumor 1
+3 more
GLikely benign
WT1
Single nucleotide variant
(intron variant)
Nephrotic syndrome, type 4
+6 more
GBenign/Likely benign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Nephrotic syndrome, type 4
+8 more
GBenign/Likely benign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Frasier syndrome
+3 more
GLikely benign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Meacham syndrome
+8 more
GBenign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Nephrotic syndrome, type 4
+7 more
GConflicting classifications of pathogenicity
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Nephroblastoma
+8 more
GBenign
LOC107982234, WT1
(G65R)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+9 more
GConflicting classifications of pathogenicity
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Meacham syndrome
+9 more
GBenign/Likely benign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Nephrotic syndrome, type 4
+9 more
GBenign/Likely benign
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