Original source

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

A/G | Ambiguity code: R

Chromosome 5:150053835 (forward strand) | View in location tab


with dbSNP rs376905470 (A/-)

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 8 transcripts and 1 regulatory feature.

Variant displays