Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.32 (A)
Location

Chromosome 4:47355396 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58273070

This variant has 3 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip, Illumina_HumanOmni1-Quad, Illumina_Human660W-quad

About this variant

This variant overlaps 2 transcripts and has 2761 sample genotypes.

Variant displays