Original source

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

Alleles
ACAG/-
Location

Chromosome 11:69624338-69624341 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.69624338_69624341delACAG

Variation displays