Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
AACTT/-|MAF: 0.28 (-)
Location

Chromosome 4:54227623-54227627 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs144906182

HGVS names

This variant has 3 HGVS names - Show

About this variant

Variant displays