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Chunk #9 — RESULTS — Genome-wide SNP association: primary analyses

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A genome-wide scan for common alleles affecting risk for autism.
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P ≤ 5 × 10−4.bBold emphasis denotes SNPs discussed.cTop association signal reported only; additional signal at reporting threshold for markers in strong LD include rs6079536, rs6079537, rs6079540, rs6079544, rs6074787, rs10446030, rs6079553, rs4814324, rs6074798, rs980319 (Supplementary Material, Table S2).dOdds ratio based on the minor allele.