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 (AT) does not match the Ensembl reference base (A) at this location.
Chromosome 10:52769917 (forward strand) | View in location tab
This variation has 6 HGVS names - click the plus to show
This variant overlaps 5 transcripts.