Original source

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

G/A/T | Ancestral: T | Ambiguity code: D | MAF: 0.20 (T)

Chromosome 3:58427942 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs3181868, rs1126698

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

This variant overlaps 40 transcripts and has 2507 sample genotypes.

Variant displays