Original source

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

Alleles
G/A|Ambiguity code: R|MAF: 0.13 (G)
Location

Chromosome 11:89922329 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59154156, rs34355950

HGVS name

11:g.89922329G>A

About this variant

This variant overlaps 5 transcripts and has 2775 sample genotypes.

Variant displays