Original source

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

G/T | Ancestral: T | Ambiguity code: K | MAF: 0.47 (G)

Chromosome 11:108368901 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs664329, rs3202133

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 11 transcripts, has 3874 sample genotypes and is mentioned in 3 citations.

Variant displays