This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP
Note: The reference base for this variant (A) does not match the Ensembl reference base (T) at this location.
Chromosome 21:32008126 (forward strand) | View in location tab
This variation has assays on: Illumina_HumanOmni1-Quad