Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 5:139330173 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

This variant has 9 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_Human610_Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 15 transcripts and has 1 sample genotype.

Variant displays