Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.03 (C)
Location

Chromosome 16:30748227 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs58186622

This variant has 2 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip, Illumina_HumanOmni1-Quad

About this variant

Variant displays