This variant has been flagged
Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP
Note: The reference base for this variant (A) does not match the Ensembl reference base (T) at this location.
Chromosome 16:20336704 (forward strand)|View in location tab
This variant has 19 HGVS names - Show
This variant has assays on: Illumina_HumanOmni1-Quad