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
This variation has 11 HGVS names - click the plus to show