Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.36 (G)

Chromosome 13:33022051 (forward strand) | View in location tab


with HGMD-PUBLIC CS043366

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs483961

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 2 transcripts, has 2776 sample genotypes and is mentioned in 3 citations.

Variant displays