Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.27 (C)
Location

Chromosome 9:122213873 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs58926937

This variant has 9 HGVS names - click the plus to show

About this variant

Variant displays