INHBB locus variants identified in a sample of the Australian cohort (n = 96).
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Identified variants were genotyped in Australian individuals passing GWAS quality control criteria (n = 1,078). Novel variants submitted to dbSNP are assigned with their ‘ss’ submission ID number.*Fisher's exact test p-value.1Major allele/Minor allele.2Hardy-Weinberg equilibrium p-value.3Preeclampsia dataset allele discordant to reference template allele.
创建时间：
2015-12-02
