This variation maps to 7 locations
Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
This variation maps to 7 genomic locations; None selected
This variation has 6 synonyms - click the plus to show
This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5
This variant has 1094 individual genotypes.