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 3 genomic locations; None selected
This variation has 2 synonyms - click the plus to show
This variation has assays on: Illumina_ExomeChip
This variant has 2 individual genotypes.