Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.33 (G)

Chromosome 9:99150189 (forward strand) | View in location tab


with HGMD-PUBLIC CR102176

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 6 transcripts, has 3901 sample genotypes and is mentioned in 15 citations.

Variant displays