数据链接：
官方服务：
资源简介：
Human genetic variants with dbSNP and pseudoDB
应用场景：
创建时间：
2023-01-05
相关数据集
European LDL GWAS MendelVar example
MendelVar annotation results for Teslovich et al. (2010) LDL GWAS.Detailed description of the output files in the "Results" section of MendelVar tutorial at:https://www.notion.so/mendelvar/MendelVar-t
NIAID Data Ecosystem90
Variants with unknown function in cases with 17p loss.
MAF: minor allele frequency (source: dbSNP).Variants with unknown function in cases with 17p loss.
Figshare2015-12-02 更新30
Additional file 2: of Vcfanno: fast, flexible annotation of genetic variants
External Lua script to compute allele frequency confidence intervals. (TXT 439 bytes)
Figshare2016-12-15 更新20
Titre GWAS output
Output of GWAS for titre, including effect size and p-values for each SNP. Can be used as input for geneticvariation_and_GWASannotate.R to look at significant SNPs (based on gwas.titre.significance.pe
Figshare2018-04-18 更新30
Table4_TRmir: A Comprehensive Resource for Human Transcriptional Regulatory Information of MiRNAs.CSV
MicroRNAs (miRNAs) are small non-coding RNAs, which play important roles in regulating various biological functions. Many available miRNA databases have provided a large number of valuable resources f
NIAID Data Ecosystem30
