This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Note: The reference base for this variant (CCCAGGGCTCCT) does not match the Ensembl reference base (C) at this location.
Chromosome 1:16986750 (forward strand) | View in location tab
This variation has 13 HGVS names - click the plus to show