Original source

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

Alleles
ACAG/-
Location

Chromosome 11:69809570-69809573 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.69809570_69809573delACAG

Variation displays