Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson's disease risk.

Nat Aging · 2025 · PMC11839463 · PMID 39572736

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nominally significantP = 9.46 × 10 −6actually significant

We also observed a nominally significant association at ATP5B (OR = 0.19, 95% CI = 0.08–0.43, P = 9.46 × 10 −6 ), but this association was not consistent in the South Korean dataset (Extended Data Fig. 7 ).

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