Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.20 (G)

Chromosome 3:46368545 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs62246126

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts, has 2555 sample genotypes and is mentioned in 2 citations.

Variant displays