Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.40 (A)
Location

Chromosome 3:49902154 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

Variant displays