Original source

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

T/A/G | Ancestral: T | Ambiguity code: D

Chromosome 13:27621426 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 22 transcripts and 1 regulatory feature.

Variant displays