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GWAS summary statistics from the Psychiatric Genomics Consortium (PGC)
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创建时间：
2021-05-26
相关数据集
Single-nucleotide polymorphisms (SNPs) detected at the TGR5 locus by complete resequencing of the gene (exons, introns, and untranslated regions) in 267 Norwegian PSC patients and 274 healthy controls.
*NCBI build 36. †Resides in exon 2 as depicted in Figure 1, but shorter variants of exon 2 (which do not include the affected nucleotide) have been reported. Alleles = major/minor allele defined from
NIAID Data Ecosystem30
Top ten Pedigree Disequilibrium Test results for categorical diagnoses of Schizophrenia.
For each gene, Chr/Mb denotes chromosome and genomic position (Megabases), dbSNP is the rs-identifier for the assayed SNP, and Nuc is the nucleotide substitution at a SNP. Frqassoc and Z-scores are wi
Figshare2015-12-02 更新20
Summary of regression analysis comparing SNP association with Cases against controls including genes within 50kb of SNPs.
Summary of regression analysis comparing SNP association with Cases against controls including genes within 50kb of SNPs.
Figshare2023-09-27 更新10
Frequencies of the haplotypes formed by rs12150079, rs9909593, rs907091 and rs2872507 SNPs in SLE patients and healthy control individuals.
Frequencies of the haplotypes formed by rs12150079, rs9909593, rs907091 and rs2872507 SNPs in SLE patients and healthy control individuals.
NIAID Data Ecosystem20
Additional file 2 of Multiple trait association analysis revealed common genetic loci between lung cancer and heart failure
Supplementary Material 2.
Figshare2026-01-12 更新10
