Original source

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

Alleles
A/- | Ancestral: A | MAF: 0.03 (-)
Location

Chromosome 11:69809513 (forward strand) | View in location tab

Most severe consequence
HGVS name

11:g.69809513delA

Variation displays