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 (C) does not match the Ensembl reference sequence (GT) at this location.
Chromosome 17:27797578-27797579 (forward strand) | View in location tab
This variation has 5 HGVS names - click the plus to show
This variant overlaps 7 transcripts.