Original source

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

Alleles
GATTC/-
Location

Chromosome 11:18401458-18401462 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 17 HGVS names - click the plus to show

Variation displays