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Dryad2017-01-01 更新2026-04-13 收录

遗传关联研究

疾病遗传易感性

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Genotype frequencies of rs1337185, rs5275, rs5277, rs7575934, rs3213718 and rs162509 in controls and cases

创建时间：

2017-01-01

The South Asian genome: Low Coverage Whole Genome Sequencing

南亚人群基因组变异

疾病遗传易感性

The genetic sequence variation of people from the Indian subcontinent who comprise one-quarter of the worldâs population, is not well described. The data provides the first c

NIAID Data Ecosystem90

Replication of our results in FinnGen MDD sample.

遗传关联研究

神经精神疾病GWAS

MDD: Major depressive disorder. P-value of binomial test of conjFDR and condFDR. (XLSX)

Figshare2022-05-13 更新40

Associations between TPH2 , GRIN3A , and GRM6 genotypes and QoL of participants.

遗传关联研究

生活质量评估

Associations between TPH2, GRIN3A, and GRM6 genotypes and QoL of participants.

NIAID Data Ecosystem40

Serum anti-glycan-antibodies in relatives of patients with inflammatory bowel disease

炎症性肠病血清学诊断

遗传关联研究

Background Serum anti-glycan antibodies are a promising tool for differential diagnosis, disease stratification and prediction of Crohn’s disease (CD). To investigate possible heritability of the mark

NIAID Data Ecosystem50

Association between SNPs from fourteen loci and type 2 diabetes in the Chinese.

遗传关联研究

2型糖尿病遗传

The OR with 95% CI shown is for the risk allele. Pallele is the P value for comparison of the allele distribution between the cases and controls. Pgenotype is the P value for comparison of genotype di

NIAID Data Ecosystem40

DATA for open access

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