Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.06 (A)

Chromosome 4:110617671 (forward strand) | View in location tab


with HGMD-PUBLIC CR043663

Most severe consequence
3 prime UTR variant
Evidence status

Clinical significance


Archive dbSNP rs58434028

This variant has 10 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 15 transcripts, has 3545 sample genotypes and is associated with 1 phenotype.

Variant displays