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 (AT) does not match the Ensembl reference base (T) at this location.
Chromosome 1:91712124 (forward strand) | View in location tab
This variation has 15 HGVS names - click the plus to show