Original source

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

Alleles
AC/- | MAF: 0.04 (-)
Location

Chromosome 11:69809515-69809516 (forward strand) | View in location tab

Most severe consequence
HGVS name

11:g.69809515_69809516delAC

About this variant

This variant overlaps 1 transcript and has 1092 individual genotypes.

Variation displays