This variation maps to 8 locations
Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
This variation maps to 8 genomic locations; None selected
This variation has 2 synonyms - click the plus to show
This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5
This variant overlaps 1 transcript.