Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.49 (G)
Location

Chromosome 8:127415816 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs57666755

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 4 transcripts and has 3694 sample genotypes.

Variant displays