Lack of an association between SCFD1 rs10139154 polymorphism and amyotrophic lateral sclerosis.

Mol Med Rep · 2022 · PMC8915390 · PMID 35234271

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possibly significantno p-value reported

In a 2016 GWAS on patients with ALS, the SCFD1 rs10139154 polymorphism was initially reported as a possibly significant genetic marker ( 27 ).

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