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 (CTAT) does not match the Ensembl reference base (T) at this location.
Chromosome 6:52476761 (forward strand) | View in location tab
This variation has 7 HGVS names - click the plus to show
This variant overlaps 6 transcripts.