This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP
Note: The reference base for this variant (C) does not match the Ensembl reference base (A) at this location.
Chromosome 2:104854218 (forward strand) | View in location tab
This variation has 3 HGVS names - click the plus to show
This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5
This variant overlaps 15 transcripts.