RS781540048 HTRA2

Health Risk Chr 2:74531866
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Associated Conditions
Parkinson disease 13
autosomal dominant
susceptibility to
Parkinson disease 13
autosomal dominant
susceptibility to
Other Variants in HTRA2
rs186272815 rs1411383758 rs2529880282 rs779457274 rs2529909206 rs372441631 rs2104369249 rs1407675367 rs2104374324 rs1675486182
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