Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.18 (G)
Location

Chromosome 5:161848296 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 2505 sample genotypes and is mentioned in 3 citations.

Variant displays