Original source

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

Alleles
A/G|Ambiguity code: R|MAF: 0.18 (G)
Location

Chromosome 6:32643157 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs9272922

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, has 2505 sample genotypes and is mentioned in 2 citations.

Variant displays