Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/- | Ancestral: A
Location

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

Most severe consequence
HGVS name

11:g.69809513delA

About this variant

This variant overlaps 1 transcript.

Variation displays