In addition, we found that 131 phenotypes in the UKB cohort and 262 phenotypes in the FinnGen cohort were suggested to be nominally significant, including alcohol-related diseases, congenital anomalies, infectious diseases, injuries and poisonings, mental disorders, neoplasms, pregnancy complications, sense organs, and dermatologic, digestive, endocrine/metabolic, genitourinary, musculoskeletal, neurological, hematopoietic, respiratory, or circulatory system problems (see Supplementary Table S10 ).
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Comprehensive Proteomic Profiling of Exfoliation Glaucoma Via Mass Spectrometry Reveals SVEP1 as a Potential Biomarker.
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