This variation has been flagged
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 8 synonyms - click the plus to show
This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni1-Quad
This variant has 1110 individual genotypes.