Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.39 (G)

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


with HGMD-PUBLIC CS043366

Most severe consequence
Evidence status


Archive dbSNP rs483961

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

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 2 transcripts, has 1373 individual genotypes and is mentioned in 3 citations.

Variation displays