This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP
Note: The reference base for this variant (C) does not match the Ensembl reference base (A) at this location.
Chromosome 7:116558117 (forward strand) | View in location tab
This variation has 7 HGVS names - click the plus to show