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 (A) does not match the Ensembl reference sequence (TT) at this location.
Chromosome 5:68254847-68254848 (forward strand) | View in location tab
Archive dbSNP rs1643921
This variation has 9 HGVS names - click the plus to show