Original source

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

Alleles
A/G | Ambiguity code: R
Location

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

Co-located

with dbSNP rs376905470 (A/-)

Most severe consequence
 
3 prime UTR variant

This variant has 3 HGVS names - click the plus to 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