Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.21 (G)
Location

Chromosome 11:22193357 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Clinical significance

Synonyms

This variant has 2 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 2511 sample genotypes and is associated with 1 phenotype.

Variant displays