Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.02 (T)
Location

Chromosome 11:18395145 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs386434015

This variant has 17 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

Variant displays