Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.25 (A)

Chromosome 13:33020990 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs529231

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, has 2508 sample genotypes and is mentioned in 3 citations.

Variant displays