Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 13:19957198 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

13:g.19957198G>A

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

Variant displays