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 20:58650540 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

20:g.58650540G>A

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 21 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays