This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Note: The reference base for this variant (C) does not match the Ensembl reference base (G) at this location.
Chromosome 22:23310360 (forward strand) | View in location tab
This variation has 2 synonyms - click the plus to show
This variation has 19 HGVS names - click the plus to show