Original source

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

Alleles
A/C/G | Ancestral: A | Ambiguity code: V
Location

Chromosome 11:18394570 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant

This variant has 28 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 46 transcripts and 1 regulatory feature.

Variant displays