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 (G) does not match the Ensembl reference sequence (TA) at this location.
Chromosome 11:116836621-116836622 (forward strand) | View in location tab
This variation has 16 HGVS names - click the plus to show
This variant overlaps 22 transcripts.