Original source

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

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2604 sample genotypes.

Variant displays