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Browse Data
Variants
Methylation
HLA
PheWeb
Metabolites
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Variant
ID
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Database
TWB1 array (GRCh37)
TWB1 array imputed (GRCh38)
TWB2 array (GRCh38)
TWB2 array imputed (GRCh38)
TWB1 and TWB2 imputed combined (GRCh38)
Whole genome sequence: Illumina (GRCh38)
Clinical significance
Pathogenic
Likely pathogenic
Drug response
Variant consequence
Predicted loss-of-function
Missense / Inframe INDEL
Synonymous
Other
