RS776155094 WT1
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What This Variant Does
"CLNSIG=4
Associated Conditions
Precursor B-cell acute lymphoblastic leukemia
Drash syndrome
Frasier syndrome
Wilms tumor 1
11p partial monosomy syndrome
WT1-related disorder
6 conditions
Inborn genetic diseases
Precursor B-cell acute lymphoblastic leukemia
Drash syndrome
Frasier syndrome
Wilms tumor 1
11p partial monosomy syndrome
WT1-related disorder
6 conditions
Other Variants in WT1