Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.49 (A)
Location

Chromosome 11:119184653 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58180459

HGVS name

11:g.119184653A>G

About this variant

This variant overlaps 22 transcripts and has 2508 sample genotypes.

Variant displays