Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.09 (A)
Location

Chromosome 5:135028725 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3191665, rs11539694

This variant has 3 HGVS names - click the plus to show

About this variant

Variant displays