Original source

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

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

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

Most severe consequence
3 prime UTR variant
Evidence status


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