This variant has been flagged
Variants (including SNPs and indels) imported from dbSNP (release 144)|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
dbSNP rs369831603 (-/T/TT/TTT)
This variant has 11 HGVS names - Show
This variant overlaps 24 transcripts.