Original source

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

Alleles
A/-|Ancestral: A|MAF: 0.01 (-)
Location

Chromosome 2:189783268 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs369571586, rs140337249

HGVS names

This variant has 8 HGVS names - Show

About this variant

Variant displays