RS2133106426 WT1

Health Risk Chr 11:32435185
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Associated Conditions
Wilms tumor 1
11p partial monosomy syndrome
Drash syndrome
Frasier syndrome
Inborn genetic diseases
Wilms tumor 1
11p partial monosomy syndrome
Drash syndrome
Frasier syndrome
Inborn genetic diseases
Other Variants in WT1
rs587776573 rs587776574 rs587776575 rs121907900 rs121907901 rs121907902 rs28941778 rs121907903 rs121907904 rs587776576
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