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

Co-located variant

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