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 (TTG) does not match the Ensembl reference sequence (TT) at this location.
Chromosome 6:32643422-32643423 (forward strand) | View in location tab
Archive dbSNP rs9279937
This variation has 7 HGVS names - click the plus to show
This variant overlaps 12 transcripts.