RS387906942 HTRA2

Health Risk Chr 2:74530433
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What This Variant Does
"CLNSIG=255
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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