Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.43 (G)
Location

Chromosome 11:45960800 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61539465, rs56616800

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

Variant displays