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 (CC) at this location.
Chromosome 22:23315694-23315695 (forward strand) | View in location tab
Archive dbSNP rs1042646
This variation has 9 HGVS names - click the plus to show