nominally significantP < 1 × 10 −4
From the common single-nucleotide variants (SNVs) analysis, we identified the abnormal nominally significant ( P < 1 × 10 −4 ) common SNVs enriched in PTBP3 gene.
From the common single-nucleotide variants (SNVs) analysis, we identified the abnormal nominally significant ( P < 1 × 10 −4 ) common SNVs enriched in PTBP3 gene.