Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D | MAF: < 0.01 (T)
Location

Chromosome 20:46118081 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

This variant has 4 HGVS names - click the plus to show

About this variant

Variant displays