Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.34 (G)
Location

Chromosome 11:66053202 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs61232781

This variant has 11 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

Variant displays