Original source

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

G/A/T | Ancestral: A | Ambiguity code: D | MAF: 0.09 (A)

Chromosome 4:73981160 (forward strand) | View in location tab


with dbSNP rs751821210 (G/-)

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs58449024

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 2 transcripts and has 3452 sample genotypes.

Variant displays