Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 20:46117926 (forward strand) | View in location tab

Most severe consequence

This variation has 2 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ImmunoChip, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 9 transcripts and has 269 individual genotypes.

Variation displays