Original source

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

This variant has 4 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

Variant displays