This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP
Note: The reference sequence for this variant (C) does not match the Ensembl reference sequence (CG) at this location.
Chromosome 11:1253073-1253074 (forward strand) | View in location tab
Archive dbSNP rs2077075
This variation has 7 HGVS names - click the plus to show