Original source

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

Alleles
-/GAGCTTCCGCCGCCG
Location

Chromosome 17: between 40819117 and 40819118 (forward strand) | View in location tab

Most severe consequence

This variation has 4 HGVS names - click the plus to show

Variation displays