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 (C) does not match the Ensembl reference sequence (GCGCGCGCGC) at this location.
Chromosome 11:27659649-27659658 (forward strand) | View in location tab
with dbSNP rs202011320 (GCGCGCGCGC/-)
Archive dbSNP rs11602143
This variation has 51 HGVS names - click the plus to show
This variant overlaps 54 transcripts.