Variant Call Format
Countries that developed this resource United Kingdom
How to cite this record FAIRsharing.org: VCF; Variant Call Format; DOI: https://doi.org/10.25504/FAIRsharing.cfzz0h; Last edited: Jan. 8, 2019, 1:28 p.m.; Last accessed: May 06 2021 10:20 a.m.
Record updated: Aug. 12, 2016, 11:44 a.m. by The FAIRsharing Team.
|online documentation||http://samtools.github.io/hts-specs/VCFv ...|
|online documentation||http://samtools.github.io/hts-specs/VCFv ...|
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ClinVar is a freely accessible, public archive of reports of the relationships among human variations and phenotypes, with supporting evidence. ClinVar thus facilitates access to and communication about the relationships asserted between human variation and observed health status, and the history of that interpretation. ClinVar processes submissions reporting variants found in patient samples, assertions made regarding their clinical significance, information about the submitter, and other supporting data. The alleles described in submissions are mapped to reference sequences, and reported according to the HGVS standard. ClinVar then presents the data for interactive users as well as those wishing to use ClinVar in daily workflows and other local applications. ClinVar works in collaboration with interested organizations to meet the needs of the medical genetics community as efficiently and effectively as possible.
RNA Binding Protein Variant Database
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Dog Genome SNP Database
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Japanese Genotype-phenotype Archive
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The Triticeae Toolbox
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Alliance of Genome Resources
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The International Genome Sample Resource
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National Cancer Institute's Genomic Data Commons
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The Wellcome Trust, UK (Charitable foundation)
WT104947/Z/14/Z (The Wellcome Trust, UK)