Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.21 (T)
Location

Chromosome 4:73869433 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs72501281

HGVS names

This variant has 3 HGVS names - Show

About this variant

Variant displays