Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.34 (A)
Location

Chromosome 4:3494423 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3172611, rs59164653

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 6 transcripts and has 3696 sample genotypes.

Variant displays