MSDD overview
MSDD (MiRNA SNP Disease Database) is a manually curated database that provides comprehensive experimentally supported associations among microRNAs (miRNAs), single nucleotide polymorphisms (SNPs) and human diseases. SNPs in miRNA-related functional regions such as mature miRNAs, promoter regions, pri-miRNAs, pre-miRNAs and target gene 3'-UTRs, collectively called “miRSNPs”, represent a novel category of functional molecules. miRSNPs can lead to miRNA and its target gene dysregulation, and resulting in susceptibility to or onset of human diseases. MSDD is devoted to collecting and storing the latest experimentally supported miRNA–SNP-disease associations. MSDD currently documents 525 associations among 182 human miRNAs, 197 SNPs, 153 genes and 164 human diseases through a review of more than 2000 published papers.
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e.g. SNP "rs2910164", Gene "BRCA1", miRNA "miR-146a", Disease "lung cancer"

Currently, users can
Browse the experimentally supported miRNA-SNP-disease association data.
Search miRNA-SNP-disease associations by particular keywords.
Download the experimentally supported miRNA-SNP-disease association data.
Submit new entries to the MiRNA SNP Disease Database.
Citation:  MSDD: a manually curated database of experimentally supported associations among miRNAs, SNPs and human diseases

Ming Yue†, Dianshuang Zhou†, Hui Zhi†, Peng Wang†, Yan Zhang, Yue Gao, Maoni Guo, Xin Li, Yanxia Wang, Yunpeng Zhang*, Shangwei Ning* and Xia Li*
Nucl. Acids Res. (2017)

Last updated on June, 2017

Formally launched on January, 2017
LincSNP 2.0            Lnc2Cancer

miRSponge             LncACTdb
Li X:

Ning S: