Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)
Location

Chromosome 11:2160980 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

This variant has 7 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 18 transcripts, 1 regulatory feature, has 2506 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays