Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.06 (A)
Location

Chromosome 16:31180161 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs52809394, rs58282123

This variant has 9 HGVS names - click the plus to show

This variant has assays on 10 chips - click the plus to show

About this variant

Variant displays