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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WT1
Deletion
(intron variant)
not provided
GUncertain significance
WT1
Single nucleotide variant
(synonymous variant +2 more)
Nephrotic syndrome, type 4
+8 more
GConflicting classifications of pathogenicity
WT1
Single nucleotide variant
(synonymous variant +2 more)
Nephrotic syndrome, type 4
+8 more
GBenign
WT1
Single nucleotide variant
(synonymous variant +2 more)
not provided
+4 more
GConflicting classifications of pathogenicity
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
WT1-related condition
+9 more
GBenign
LOC107982234, WT1
Single nucleotide variant
(synonymous variant +1 more)
Drash syndrome
+8 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)
Drash syndrome
+9 more
GBenign/Likely benign
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