RS121909715 GSN

Health Risk Chr 9:121310819
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What This Variant Does
"rs121909715, also known as c.520G&gt
Associated Conditions
Finnish type amyloidosis
Inborn genetic diseases
Finnish type amyloidosis
Finnish type amyloidosis
Inborn genetic diseases
Finnish type amyloidosis
Other Variants in GSN
rs528604896 rs146956976 rs372713895 rs142828669 rs147554026 rs886063405 rs764841269 rs138068754 rs761824852 rs750132751
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