Original source

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

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

Chromosome 3:16604687 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

Variant displays