Barely Significant
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Association study of GBA1 variants with MSA based on comprehensive sequence analysis -Pitfalls in short-read sequence analysis depending on the human reference genome.

J Hum Genet · 2024 · PMC11599039 · PMID 39020124

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The combined allele frequency of all the pathogenic variants in the MSA cases was higher than those described in the previous report [ 10 ], which, however, did not reach statistical significance.

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