Original source

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

Alleles
G/C|Ancestral: C|Ambiguity code: S|MAF: 0.41 (G)
Location

Chromosome 16:56914069 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs61049491

HGVS names

This variant has 4 HGVS names - Show

About this variant

Variant displays