Original source

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

A/G/T | Ancestral: A | Ambiguity code: D | MAF: 0.17 (G)

Chromosome 9:27546830 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs117637811, rs3174187

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 6 transcripts, has 3691 sample genotypes and is mentioned in 2 citations.

Variant displays