Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.01 (G)
Location

Chromosome 17:27756893 (forward strand)|View in location tab

Co-located variant

dbSNP rs56090761 (A/G)

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs386490305

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

Variant displays