Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
-/AT
Location

Chromosome 1: between 77944321 and 77944322 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 9 HGVS names - click the plus to show

Variation displays