ClinVar is an archive for assertions of clinical significance made by the submitters. The level of review supporting the assertion of clinical significance for ...

Simple ClinVar ... Simple ClinVar was developed to provide gene- and disease-wise summary statistic based on all available genetic variants from ClinVar. How many ...

Clinvar class is the clinical significance value given by ClinVar database:

Müddət: 6:26
Dərc edildi: 9 мар 2016

ClinVar is a freely accessible, public archive of reports of the relationships among human variations and phenotypes, with supporting evidence. ClinVar thus ...

20 ној 2017 · INTRODUCTION. ClinVar (1,2) is a freely available, public archive of human genetic variants and interpretations of their significance to disease ...

Search for genes and functional terms extracted and organized from over a hundred publicly available resources.

1 ијн 2018 · A recent unbiased study found inflation of the genetic risk of endocrine tumour syndromes in the genotype–phenotype database ClinVar.

ClinVar annotations ... This dataset contains annotations from ClinVar that were loaded into Cloud Life Sciences for use in sample annotation pipelines. The ...

ClinVar — один из самых полезных инструментов, позволяющих узнать больше о том, что ваши SNP могут значить для здоровья. Это открытый общедоступный архив, целью ...