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 () at this location.
Chromosome 11: between 112095868 and 112095869 (forward strand) | View in location tab
with dbSNP rs369831603 (-/T)
This variation has 11 HGVS names - click the plus to show
This variant overlaps 24 transcripts.