Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.06 (C)
Location

Chromosome 11:18394766 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

HGVS names

This variant has 17 HGVS names - Show

About this variant

Variant displays