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CHRIS data
CHRIS baseline data
Genomics (CHRIS baseline)
Genomic variants (CHRIS baseline)
Whole-exome sequencing imputation (CHRIS baseline)
WES imputed variants GRCh37 (vcf)
WES imputed variants GRCh37 (vcf)
x0gn41
WES imputed variants GRCh37 (vcf)
Type
Boolean
Unit
Version
1.0.0.3
Groups
No groups.