RS28941779 WT1

Health Risk Chr 11:32392026
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What This Variant Does
"rs28941779, also known as Phe392Leu or F392L, is a SNP in the WT1 gene on chromosome 11. A report li...
Associated Conditions
Frasier syndrome
Frasier syndrome
Other Variants in WT1
rs587776573 rs587776574 rs587776575 rs121907900 rs121907901 rs121907902 rs28941778 rs121907903 rs121907904 rs587776576
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