Clinical SNP Variants

Downloadable File
Organism: 
Homo sapiens (Human)
File: 
Binary Data clinvar.vcf.gz
Index: 
Binary Data clinvar.vcf.gz.tbi
Program, Pipeline Name or Method Name: 
NCBI ClinVar dataset
Program, Pipeline or Method version: 
vcf_GRCh38
Source Name: 
NCBI
Source URI: 
ftp://ftp.ncbi.nih.gov/pub/clinvar/vcf_GRCh38/
Time Executed: 
02/28/2018
Materials & Methods (Description and/or Program Settings): 
ClinVar variants with precise endpoints. Each variant is represented by a single location in the reference assembly for GRCh38.