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 (AAAG) does not match the Ensembl reference base (A) at this location.
Chromosome 5:96775265 (forward strand) | View in location tab
Archive dbSNP rs34915580
This variation has 7 HGVS names - click the plus to show