ClinVar: public archive of interpretations of clinically relevant variants


ClinVar ( at the National Center for Biotechnology Information (NCBI) is a freely available archive for interpretations of clinical significance of variants for reported conditions. The database includes germline and somatic variants of any size, type or genomic location. Interpretations are submitted by clinical… (More)
DOI: 10.1093/nar/gkv1222


3 Figures and Tables