Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.19 (A)
Location

Chromosome 20:54160353 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

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

About this variant

Variant displays