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 12:56663421 (forward strand) | View in location tab
This variant has 7 HGVS names - Show
This variant has assays on: Illumina_Human1M-duo, Illumina_Human610_Quad