ClinVar - ClinGen | Clinical Genome Resource
The ClinVar variation report
A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer | Nature Genetics
Using dbSNP and ClinVar to Classify Gene Variants
Breakdown of variants found in the Leiden open-source variation... | Download Scientific Diagram
PLOS Computational Biology: GEMINI: Integrative Exploration of Genetic Variation and Genome Annotations
DECIPHER v11.12: Mapping the clinical genome
The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting | SpringerLink
DisGeNET - a database of gene-disease associations
The Clinical Genome (ClinGen) Resource
CCEPAS: the creation and validation of a fast and sensitive clinical whole exome analysis pipeline based on gene and variant ranking
Frontiers | Workflow for the Implementation of Precision Genomics in Healthcare | Genetics
Characterizing and Displaying Genetic Variants for Clinical Action Workshop
Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes | Nature Communications
Technical desiderata for the integration of genomic data with clinical decision support - ScienceDirect
Variation Viewer
HuVarBase: A human variant database with comprehensive information at gene and protein levels | PLOS ONE
Comparison of Open-access Databases for Clinical Variant Interpretation in Cancer: A Case Study of MDS/AML | Cancer Genomics & Proteomics
Clinical Bioinformatics in Precise Diagnosis of Mitochondrial Disease - Clinics in Laboratory Medicine
Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer - The Journal of Molecular Diagnostics
InSiGHT variants databases - InSiGHT
Variant Harmonization Process Overview Pre-launch and post-launch... | Download Scientific Diagram
Variation Viewer
Genetic Testing For Hereditary Disease | QIAGEN
DoCM: a database of curated mutations in cancer | Nature Methods
ClinGen — The Clinical Genome Resource | NEJM
