Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.12 (A)
Location

Chromosome 11:6388560 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

11:g.6388560G>A

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 10 transcripts and has 3661 sample genotypes.

Variant displays