This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Note: The reference sequence for this variant (G) does not match the Ensembl reference sequence () at this location.
Chromosome 16: between 28903508 and 28903509 (forward strand) | View in location tab
This variation has 9 HGVS names - click the plus to show
This variant overlaps 16 transcripts.